IN-DATE
AR-8988-CP: Arthrex FiberLock Suspension Implant Kit
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| Price: | $1,499.00 per box of 1 |
|---|---|
| Quantity: | |
| In Stock: | 2 box of 1 |
| Expiration: | 03-2029 |
Additional Details
Arthrex AR-8988-CP FiberLock Suspension System
Arthrex AR-8988-CP FiberLock Suspension System is a sterile implant kit designed for carpometacarpal (CMC) suspensionplasty of the thumb. The system uses a DX FiberTak anchor and 3.5 mm DX SwiveLock SL anchor with dedicated drilling and guide instrumentation to create a suture-based suspension construct for treatment of thumb CMC joint pathology.
Product Code: AR-8988-CP
- Manufacturer: Arthrex
- Product Name: FiberLock Suspension System
- Brand / Product Family: FiberLock
- Device Type: CMC suspensionplasty implant system
- Primary Anchor: DX FiberTak Anchor
- Secondary Anchor: 3.5 mm DX SwiveLock SL Anchor
- FiberTak Drill Diameter: 1.6 mm
- FiberTak Guidewire Diameter: 1.35 mm
- SwiveLock Drill Diameter, Soft Bone: 2.7 mm
- SwiveLock Drill Diameter, Normal Bone: 3.0 mm
- SwiveLock Guidewire Diameter: 1.35 mm
- Clinical Application: Thumb CMC suspensionplasty
- Procedure Type: Carpometacarpal joint reconstruction and suspensionplasty
- Specialty: Orthopedic Surgery
- Anatomical Application: Thumb / carpometacarpal joint
- Implantable: Yes
Contents
- DX FiberTak Anchor on Short Driver without Needles
- 1.35 mm Guidewire for FiberTak Anchor
- 1.6 mm FiberTak Drill
- FiberTak Drill Guide
- Free Needle
- 3.5 mm DX SwiveLock SL Anchor on Short Driver
- 2.7 mm Cannulated DX SwiveLock SL Drill Bit for Soft Bone
- 3.0 mm Cannulated DX SwiveLock SL Drill Bit for Normal Bone
- 1.35 mm Trocar-Tip Guidewires
- Drill Guide with Depth Stop
Features
- Designed for suture-based thumb CMC suspensionplasty
- DX FiberTak anchor provides soft-anchor fixation
- DX SwiveLock SL anchor provides fixation at the first metacarpal
- Dedicated drill sizes support preparation for different bone quality
- May be used as a stand-alone suspension construct or with a soft-tissue adjunct depending on surgical technique
Sterilization
- Device Packaged as Sterile: Yes
- Requires Sterilization Prior to Use: No
- Single-Use, Disposable
AccessGUDID Info
- FDA Product Code: MBI
- FDA Product Code Name: Fastener, fixation, nondegradable, soft tissue
- GMDN Term Code: 45062
- GMDN Term Name: Tendon/ligament bone anchor, non-bioabsorbable
- GMDN Term Description: A non-bioabsorbable device designed to be implanted into bone for the attachment of tendons/ligaments/soft tissues either directly or via a suture attached to the device; typically used in arthroscopic or open surgical procedures. This device is available in various designs and sizes and is made of a material that cannot be chemically degraded or absorbed via natural body processes [e.g., titanium (Ti)].
Manufacturer
Arthrex is a global leader in orthopedic surgical innovation, dedicated to helping surgeons treat their patients better. Specializing in minimally invasive orthopedic technologies, Arthrex offers a comprehensive range of solutions for sports medicine, joint preservation, and trauma. Their cutting-edge products include the Arthrex Synergy UHD4™ imaging platform, FiberTape® and FiberWire® suture systems, and BioCartilage® for joint restoration. With a strong commitment to medical education and research, Arthrex empowers surgeons with advanced tools and training, driving improved outcomes and enhancing quality of life for patients worldwide.
There is no valid manufacturer warranty on the products that Synergy Surgical sells. Any services provided by the original manufacturer of the products we sell are not available. However, Synergy Surgical offers a 100% money back guarantee (less shipping) on every item we sell within 30 days of purchase. For details, please see our Return Policy.
