# K052405: Sterling Interferenc Screw HT

- Pathway: 510(k) (Traditional)
- Applicant: Regeneration Technologies, Inc.
- Decided: Nov 16, 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.
66 later devices descend from it; 1 cites it directly.
0 of 67 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 its predicate without a number.
- (no number) STERLING® Interference Screw ST: named in the summary without a submission number

## Most influential descendants
- K072914: Natural Bridge LP Transverse Connectors (2008), 65 descendants of its own
- K120099: Range Spinal System (Mesa and Denali) (2012), 53 descendants of its own
- K120656: Everest Spinal System (2012), 43 descendants of its own
- K132757: Everest Spinal System (2013), 41 descendants of its own
- K121016: Range Spinal System (Mesa and Denali) (2012), 38 descendants of its own

## Indications for use
The STERLING® Interference Screw HT is used to provide interference fixation in anterior cruciate ligament reconstruction using a bone-tendon-bone graft; fixation during posterior cruciate ligament reconstruction utilizing a bone-tendon-bone graft.

Source page: https://510kreport.com/device/K052405
Methodology: https://510kreport.com/methodology