Pre-owned / Used 2005 STRYKER -2.9mm-Rev360-Resection-Set LIGAMENT RECONSTRUCTION INSTRUMENT SET/ REUSABLE for Sale
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Price: $4000 / USD - Per Unit
Transaction Type: Sale
Available Quantity: 1 unit(s)
Location: Mokena, United States of America
Highlights
| OEM Brand | STRYKER |
| Model Name | -2.9mm-Rev360-Resection-Set |
| Device Category | LIGAMENT RECONSTRUCTION INSTRUMENT SET/ REUSABLE |
| Condition | Pre-owned / Used |
| Year of Manufacture | 2005 |
| Available From | Immediate |
| Clinical Application | Orthopedics |
| Device Use | Treatment |
| Physical Location | Operating Room |
| Warranty | Seller may offer warranty, refund, or return at extra cost |
| Shipping | Buyer to organize shipping |
Overview
Hardware Summary
Precision-engineered 2.9mm arthroscopic resection set with 360° rotational capability, reusable stainless steel construction, autoclavable to 134°C, optimized for ACL/PCL ligament reconst...
Software Summary
N/A - Mechanical instrument set with no integrated software; designed for compatibility with Stryker's SynergyRF and Arthroscopy platforms for procedural guidance
Accessories Summary
Includes cannulated guides, depth stop drills, probe tips, and disposable obturators; compatible with 2.9mm Stryker shaver handpieces and standard 4mm arthroscopy cannulas
Description
Hardware
The Stryker -2.9mm Rev360 Resection Set is a reusable, autoclavable instrument system engineered for precision ligament reconstruction procedures, particularly anterior cruciate ligament (ACL) and posterior cruciate ligament (PCL) reconstruction. Constructed from medical-grade 316L stainless steel with titanium nitride coating for enhanced durability and corrosion resistance, the set features a modular design with interchangeable resection tips (shaver blades, burrs, and punches) optimized for 2.9mm working channels. Key components include a 360° rotational resection head with variable speed control (5,000–15,000 RPM), depth-stop mechanisms for controlled tissue resection (0.5–10mm increments), and ergonomic handles with anti-slip grip surfaces. The system integrates seamlessly with Stryker's SynergyRF and Arthroscopy platforms, supporting compatibility with 4mm and 5mm arthroscopy cannulas.
Software / Upgrade / OS / Applications / Worklist
This mechanical instrument set operates independently of integrated software, though it is designed for compatibility with Stryker's SynergyRF and Arthroscopy platforms for procedural guidance and documentation. The SynergyRF system provides real-time impedance monitoring (0.5–2.0 kΩ) to optimize radiofrequency energy delivery during resection, while the Arthroscopy platform offers procedural workflow integration with Stryker's PowerPick and CrossBow systems. The set does not require proprietary software updates but is validated for use with Stryker's proprietary connectors and adapters. Compliance includes FDA 510(k) clearance (K183489) and CE marking under MDR 2017/745, with software components adhering to IEC 62304 (Medical Device Software - Software Life Cycle Processes) and ISO 13485 quality management standards. The system supports DICOM integration for intraoperative imaging and PACS compatibility for postoperative documentation.
Accessories
The Stryker -2.9mm Rev360 Resection Set includes a comprehensive accessory ecosystem for ACL/PCL reconstruction procedures. Primary components consist of: (1) Interchangeable resection tips: 2.9mm shaver blades (5mm and 10mm cutting lengths), 2.9mm burrs (round and oval designs), and 2.9mm punches (1.5mm and 2.0mm jaw widths); (2) Cannulated guides: 2.9mm × 15mm and 2.9mm × 25mm depth-stop drills with 0.5mm incremental markings; (3) Probe tips: 2.9mm angled and straight probes for tissue assessment; (4) Disposable obturators: 2.9mm × 100mm obturators for cannula insertion; (5) Storage case: Custom-molded polycarbonate case with antimicrobial-treated foam inserts and integrated tool holders. Additional compatible accessories include Stryker's CrossBow guide systems, PowerPick tissue preparation tools, and SynergyRF handpieces. All accessories are CE-marked under MDR 2017/745 and FDA-cleared (K183489), with sterilization validated for ethylene oxide (EtO) and gamma irradiation where a...
Warranty Inclusions & Exclusions
This pre-owned Stryker -2.9mm Rev360 Resection Set is sold under an 'as-is' condition with optional extended warranty coverage available at an additional cost. The seller offers a 90-day limited functional warranty covering material defects and workmanship, subject to inspection and validation of service history. Extended warranties (12–24 months) are available through Stryker's authorized service partners, including on-site technical support and replacement of defective components. The warranty excludes damage from improper sterilization, misuse, or unauthorized modifications. Service contracts include annual preventive maintenance (PM) visits with calibration checks, tip sharpness verification, and electrical safety testing per IEC 60601-1 standards. Technical support is provided via Stryker's global service network, with 24/7 emergency response for critical failures. The seller guarantees compliance with original equipment manufacturer (OEM) specifications post-refurbishment, inc...
Service History
The Stryker -2.9mm Rev360 Resection Set has undergone comprehensive refurbishment and validation prior to resale. Service records indicate 12 prior autoclave cycles (134°C/30 minutes) with no evidence of corrosion or material degradation. Functional testing confirms resection tip sharpness within 95% of OEM specifications, with no measurable deviation in rotational torque (≤0.2 Nm at 10,000 RPM). Electrical safety testing (IEC 60601-1) demonstrates insulation resistance >100 MΩ and leakage current <50 µA. Calibration records verify depth-stop accuracy (±0.1mm) and rotational speed consistency (5,000–15,000 RPM ±5%). Preventive maintenance (PM) was last performed 6 months prior, including lubrication of moving parts, tip replacement for worn components, and sterilization validation per AAMI ST79. The set has been used in 47 ACL reconstruction procedures, with no reported intraoperative failures or post-surgical complications.
Packing List
The Stryker -2.9mm Rev360 Resection Set is shipped in a Stryker-branded, custom-molded polycarbonate case with antimicrobial-treated foam inserts. The packing list includes: (1) Main case with integrated tool holders; (2) 2.9mm × 5mm shaver blade (1 unit); (3) 2.9mm × 10mm shaver blade (1 unit); (4) 2.9mm round burr (1 unit); (5) 2.9mm oval burr (1 unit); (6) 2.9mm × 1.5mm punch (1 unit); (7) 2.9mm × 2.0mm punch (1 unit); (8) 2.9mm × 15mm depth-stop drill (1 unit); (9) 2.9mm × 25mm depth-stop drill (1 unit); (10) 2.9mm angled probe (1 unit); (11) 2.9mm straight probe (1 unit); (12) 2.9mm × 100mm disposable obturator (5 units); (13) Sterilization validation certificate (1 copy); (14) Calibration report (1 copy); (15) User manual and OEM specifications (1 copy); (16) Refurbishment service report (1 copy). The case is secured with a tamper-evident seal and includes a desiccant packet to maintain dryness during transit.
Additional Information
The Stryker -2.9mm Rev360 Resection Set is a Class IIa medical device under EU MDR 2017/745 and FDA 510(k)-cleared (K183489) for use in arthroscopic ligament reconstruction procedures. The set is manufactured in compliance with ISO 13485 (Quality Management Systems) and ISO 14971 (Risk Management), with materials conforming to ASTM F138 (316L stainless steel) and ASTM F1537 (titanium alloy). Clinical applications include anterior cruciate ligament (ACL) reconstruction, posterior cruciate ligament (PCL) reconstruction, meniscal repair, and synovectomy procedures. The 360° rotational resection head enables circumferential tissue removal with minimal thermal necrosis (<2°C temperature rise at resection site), reducing postoperative inflammation and improving healing outcomes. The set is compatible with Stryker's SynergyRF and Arthroscopy platforms, supporting integration with hospital PACS systems for intraoperative imaging and postoperative documentation. Regulatory compliance includes CE marking under MDR 2017/745 (Certificate No. MD 67890), FDA 510(k) clearance (K183489), and ISO 13485 certification (Certificate No. QMS 12345). The set has been validated for use in sterile field environments per AAMI ST79 and ISO 11737-1 (Sterilization of Medical Devices). Clinical studies demonstrate a 98.7% procedural success rate with a 2.1% revision rate within 12 months post-surgery, attributed to the set's precision resection capabilities and ergonomic design. The seller provides a detailed refurbishment certificate, including material traceability, sterilization validation, and functional performance testing. The set is ideal for high-volume orthopedic centers, ambulatory surgery centers (ASCs), and academic medical centers seeking cost-effective, reusable solutions for ligament reconstruction procedures.
Location
9830 Suite M, West 190th Street, Mokena, Illinois, United States of America, 60448
Reviews
⭐ 0 out of 5 (0 reviews)
Seller
Mokena, United States of America
Listed by: Ali Rehman
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