# K021030: Titanium Cannulated Interference Screw

- Pathway: 510(k) (Traditional)
- Applicant: Future Medical Systems, Inc.
- Decided: Jun 25, 2002 after 88 days
- Product code: HWC (Screw, Fixation, Bone)
- 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 K010595 (2001). 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)
- K010595: DJ Orthopedics Interference Screw, Dj Orthopedics, LLC (2001) Summary page 1.

## Indications for use
To provide interference fixation of soft tissue graft and bone-tendon-bone patellar graft during cruciate ligament repair through arthroscopy or arthrotomy.

Source page: https://510kreport.com/device/K021030
Methodology: https://510kreport.com/methodology