PEEK Interference Screw
PEEK Interference Screw — a orthopedic bone screw from OrthoLimited, supplied to ISO 13485 standards for hospitals and distributors worldwide.
- SKU
- C004
- MPN
- C004
- Brand
- OrthoLimited
- Manufactured by
- OrthoLimited Inc.
- Warehouse
- EU
- Availability
- In stock
- ✓ CE marked
- ✓ ISO 13485
- ✓ Warranty included
- ✓ Worldwide shipping
Clinical overview
Product overview
What is the PEEK Interference screw?
PEEK Interference screws are used for fixation of anterior and posterior tendon repairs, are made of PEEK (Poly Ether-Ether Kethon). These screws are also used on BTB and soft tissue fixations. Fully threaded and blut screws protect the graft from laceration on insertion.
Interference screw is a popular fixation device used to rigidly fix bone-patellar tendon-bone (B-PT-B) graft both in femoral and tibial tunnels in anterior cruciate ligament (ACL) reconstruction. Parallel placement of screw is difficult in transtibially drilled femoral tunnel but always desired as it affects pullout strength of the graft. Commonly, interference screw into the femoral tunnel is inserted through the anteromedial (AM) or accessory AM portal.
These portals are not-in-line with the transtibially drilled femoral tunnel. Furthermore, these portals increase the divergence of the interference screw in the femoral tunnel. We hypothesized that interference screw placement through patellar tendon (PT) portal (through donor defect) in transtibially drilled femoral tunnel can be less divergent.
What are interference screws made of?
OrthoLimited Interference Screws are of the highest quality standard. A complete family of interference screws includes Bio-Interference Screws (primarily amorphous PLLA Full Thread), PEEK Interference Screws, Metal Interference Screws (made from titanium for femoral and tibial fixation of a soft tissue or bone-tendon grafts in cruciate ligament reconstruction procedures), and Sheath Cannulated Screws (translucent sheath).
Technical specifications
Engineering at a glance
Documentation, IFU and DOCs available on request — contact our sales team for the full regulatory file.
- Model
- C004
- Material
- medical stainless steel
- Certification
- CE, ISO 9001, ISO 13485
Documents & downloads
Regulatory paperwork & manuals
Pre-cleared documentation for this device. Full tender-pack originals are available on request.
Documents & downloads
Regulatory paperwork & manuals
This device's IFU, CE Declaration of Conformity, ISO 13485 certificate and (where applicable) FDA 510(k) clearance ship with the order. Reach out below for the pack ahead of purchase.
Get in touch
Need configuration help, certificates, or volume pricing?
Our clinical sales team will scope quantities, voltage, accessories and regulatory paperwork — usually within one business day.
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