# K100532: Versalok Peek Anchor with Orthocord Suture, Models 210818, 210819

- Pathway: 510(k) (Special)
- Applicant: Depuy Mitek, A Johnson & Johnson Company
- Decided: Mar 17, 2010 after 20 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
Longest line of descent: 4 generations back to K012125 (2001). 10 ancestors in all.
No later device cites it as a predicate yet.
0 of 11 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- K060914: Trident Anchor, Johnson & Johnson Company (2006) Summary page 1.
- K063478: Versalok Anchor with Free Strands of Orthocord Suture (210808), Ethibond Suture (210809), and Panacryl Suture (210810), Depuy Mitek, A Johnson & Johnson Company (2006) Summary page 2.
- K063479: Arthrex Pushlock, Arthrex, Inc. (2006) Summary page 1.

## Indications for use
VERSALOCK Anchor is indicated for use in the following: Shoulder: Rotor Cuff Repair, Biceps Tenodesis Knee: Medial Collateral Ligament Repair, Lateral Collateral Ligament Repair, Posterior Oblique Ligament Repair, Iliotibial Band Tenodesis; Joint Capsule Closure Elbow: Biceps Tendon Reattachment

Source page: https://510kreport.com/device/K100532
Methodology: https://510kreport.com/methodology