# K073426: Aperfix Interference Screw 7-12 MM X 20 MM; 7-12 MM X 25 MM; 7-12 MM X 30 MM

- Pathway: 510(k) (Traditional)
- Applicant: Cayenne Medical, Inc.
- Decided: Feb 19, 2008 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.
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
- K092381: Ibalance Akrfx Medial Opening Wedge Tibial System, Ifx Medial Peek Implant and Anchor, Akrfx Instrumentation (2009), 0 descendants of its own

## Indications for use
The AperFix™ Interference Screw is intended for use with bone patellar tendon bone (BPTB) grafts to provide fixation during arthroscopic or open ACL reconstruction procedures.

Source page: https://510kreport.com/device/K073426
Methodology: https://510kreport.com/methodology