# K050767: Sterling Interference Screw ST

- Pathway: 510(k) (Traditional)
- Applicant: Regeneration Technologies, Inc.
- Decided: Jun 9, 2005 after 76 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
No predicates in its family tree.
No later device cites it as a predicate yet.
0 of 1 device in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- None. The FDA summary names its predicate without a number.
- (no number) Bioscrew Absorbable Interference Screw: named in the summary without a submission number
- (no number) BioOss Anorganic Bovine Bone: named in the summary without a submission number

## Indications for use
The STERLING® Interference Screw ST is used to provide interference fixation of femoral and/or tibial tunnels in anterior cruciate ligament reconstruction using a soft tissue graft; fixation during posterior cruciate ligament reconstruction utilizing a soft tissue graft.

Source page: https://510kreport.com/device/K050767
Methodology: https://510kreport.com/methodology