# K950875: Ogden Anchor

- Pathway: 510(k) (Traditional)
- Applicant: American Medical Electronics, Inc.
- Decided: Jul 11, 1995 after 133 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.
167 later devices descend from it; 1 cites it directly.
0 of 168 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
- K972783: Biofix Biodegradable Threaded Suture Anchor (1998), 166 descendants of its own
- K982139: Biosorbfx 1.5/2.0 Bioabsorbable Fixation System (1998), 86 descendants of its own
- K993061: Stryker Leibinger Resorbable Fixation System (1999), 79 descendants of its own
- K020056: Duet Suture Anchor (2002), 78 descendants of its own
- K030388: Impact Suture Anchor. Model 433510 (2003), 77 descendants of its own

Source page: https://510kreport.com/device/K950875
Methodology: https://510kreport.com/methodology