# K123240: Speedlock Hip Knotless Fixation Implant

- Pathway: 510(k) (Traditional)
- Applicant: ArthroCare Corporation
- Decided: Feb 14, 2013 after 121 days
- Product code: MBI (Fastener, Fixation, Nondegradable, Soft Tissue)
- 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: 7 generations back to K961555 (1996). 23 ancestors in all.
No later device cites it as a predicate yet.
0 of 24 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- K120943: Speedlock Hip Knotless Fixation Implant  Speedlock Hip Drill Speedlock Hip Guide Crown Tip Speedlock Hip Pathfinder, ArthroCare Corporation (2012) Summary page 1.

## Indications for use
The SpeedLock HIP Knotless Fixation Implant is indicated for use in fixation of soft tissue to bone in the hip. Examples of such procedures include: Hip capsule repair Acetabular labrum reattachment

Source page: https://510kreport.com/device/K123240
Methodology: https://510kreport.com/methodology