# K060693: Microstrike and Allthread Peek Suture Anchor

- Pathway: 510(k) (Traditional)
- Applicant: Arthrotek, Inc.
- Decided: Jun 6, 2006 after 83 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.
27 later devices descend from it; 6 cite it directly.
0 of 28 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- None. FDA has not posted a summary or statement for it, so its predicates are not known.

## Most influential descendants
- K070389: Peek Knotless Anchors (2007), 9 descendants of its own
- K133036: Apollo Suture Anchor System and Titan Screws (2014), 7 descendants of its own
- K110230: Rog Knotless Suture Anchor (2011), 7 descendants of its own
- K110229: Rog Suture Anchor 5.5MM, 2.9MM (2011), 6 descendants of its own
- K080088: Biomet Sports Medicine Anchor Devices and Ziploop Constructs (2008), 6 descendants of its own

Source page: https://510kreport.com/device/K060693
Methodology: https://510kreport.com/methodology