# K792670: Smith Subtalar Peg

- Pathway: 510(k) (Traditional)
- Applicant: Dow Corning Wright
- Decided: Feb 22, 1980 after 57 days
- Product code: LXH (Orthopedic Manual Surgical Instrument)
- Device class: 1
- Regulation: 21 CFR 888.4540
- Recalls of this device: none
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Lineage
No predicates in its family tree.
59 later devices descend from it; 3 cite it directly.
0 of 60 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
- K960692: Subtalar Mba System (1996), 57 descendants of its own
- K071498: Subtalar Implant (2007), 32 descendants of its own
- K133636: Extremity Medical Hammertoe Device (2014), 31 descendants of its own
- K141857: CrossTie Intraosseous Fixation System (2015), 16 descendants of its own
- K031155: Osteomed Subtalar Implant System (2003), 16 descendants of its own

Source page: https://510kreport.com/device/K792670
Methodology: https://510kreport.com/methodology