# K963973: Depuy Cannulated Cross Pin Screw System

- Pathway: 510(k) (Traditional)
- Applicant: Depuy, Inc.
- Decided: Dec 16, 1996 after 74 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 K946228 (1995). 2 ancestors in all.
No later device cites it as a predicate yet.
0 of 3 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- K954630: Depuy Titanium Cross Pin Fixation System, Depuy, Inc. (1995) Summary page 1.
- K946228: Cross Pin Screw System, Depuy, Inc. (1995) Summary page 1.
- (no number) Arthrex SemiFix ACL Reconstruction System: named in the summary without a submission number

## Indications for use
The DePuy Cannulated Cross Pin Screws are intended to provide early fixation of autogenous or allogeneic tendon grafts in surgical procedures for anterior cruciate ligament (ACL) reconstruction.

Source page: https://510kreport.com/device/K963973
Methodology: https://510kreport.com/methodology