# K001228: External Fixation Anchor Pin

- Pathway: 510(k) (Traditional)
- Applicant: Immedica, Inc.
- Decided: Jul 7, 2000 after 81 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.
2 later devices descend from it; 1 cites it directly.
0 of 3 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- None. FDA lists a 510(k) statement for it but has not posted the file, so its predicates are not known.

## Most influential descendants
- K042761: Wristore Distal Radius Fracture Fixator, 4600 Series (2004), 1 descendant of its own
- K052498: Fragment Specific Fixator (2005), 0 descendants of its own

Source page: https://510kreport.com/device/K001228
Methodology: https://510kreport.com/methodology