# K071569: Allthread Peek Anchor with Tantalum Marker

- Pathway: 510(k) (Special)
- Applicant: Biomet, Inc.
- Decided: Jul 2, 2007 after 24 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
No predicates in its family tree.
15 later devices descend from it; 2 cite it directly.
0 of 16 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
- K133036: Apollo Suture Anchor System and Titan Screws (2014), 7 descendants of its own
- K080088: Biomet Sports Medicine Anchor Devices and Ziploop Constructs (2008), 6 descendants of its own
- K142230: Apollo Suture Anchor System and Titan Screws (2014), 5 descendants of its own
- K110473: Nanotack Suture Anchor 1.4MM (2011), 2 descendants of its own
- K192810: Apollo Suture Anchor System (2020), 1 descendant of its own

Source page: https://510kreport.com/device/K071569
Methodology: https://510kreport.com/methodology