# K060253: Sterling Interference Screw HT, Sterling Interference Screw ST.

- Pathway: 510(k) (Special)
- Applicant: Regeneration Technologies, Inc.
- Decided: Feb 23, 2006 after 22 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.
1 later device descends from it; 1 cites it directly.
0 of 2 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- None. The FDA summary names no predicate by number.

## Most influential descendants
- K063584: Sterling IF Screw Eyelet, Model CID3936 and Sterling Cross-Pin Eyelet, Model CID3937 (2007), 0 descendants of its own

## 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, and fixation during posterior cruciate ligament reconstruction utilizing a soft tissue graft. The STERLING® Interference Screw HT is used to provide interference fixation in anterior cruciate ligament reconstruction using a bone-tendon-bone graft, and fixation during posterior cruciate ligament reconstruction utilizing a bone-tendon-bone graft.

Source page: https://510kreport.com/device/K060253
Methodology: https://510kreport.com/methodology