# K011137: Resorbable Hammertoe Pin

- Pathway: 510(k) (Traditional)
- Applicant: Biomet, Inc.
- Decided: Jun 19, 2001 after 67 days
- Product code: JDW (Pin, Fixation, Threaded)
- 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
- K021828: Small Hammer Toe Pin (2002), 14 descendants of its own
- K100414: Protoe Endosorb Small Hammer Toe Pin (2010), 13 descendants of its own
- K100926: Arrowhead Fixation Device (2010), 10 descendants of its own
- K112675: Arrow-Lok Digital System (2011), 9 descendants of its own
- K183055: Vector Hammertoe Correction System (2019), 4 descendants of its own

Source page: https://510kreport.com/device/K011137
Methodology: https://510kreport.com/methodology