# K012270: Stryker Cross-Pinned  Interference Screw System

- Pathway: 510(k) (Traditional)
- Applicant: Stryker Endoscopy
- Decided: Sep 28, 2001 after 71 days
- Product code: JDW (Pin, Fixation, Threaded)
- Device class: 2
- Regulation: 21 CFR 888.3040
- Recalls of this device: none
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Lineage
Longest line of descent: 1 generation back to K972233 (1997). 1 ancestor in all.
No later device cites it as a predicate yet.
0 of 2 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- K972233: Stryker Wedge Interference Screw System, Stryker Endoscopy (1997) Summary page 1.

## Indications for use
The Stryker Cross-Pinned Interference Screw System is intended for use in the surgical reconstruction of the anterior cruciate ligament (ACL) deficient knee to provide interference fixation of the various ACL allografts and autografts, including the patella bone-patellar tendon-tibial bone graft complex, the semi-tendinosus tendon graft, the semi-membranosus tendon graft, and the Achilles tendon graft.

Source page: https://510kreport.com/device/K012270
Methodology: https://510kreport.com/methodology