# K951303: SFC

- Pathway: 510(k) (Traditional)
- Applicant: Medpac
- Decided: Jun 27, 1995 after 97 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.
28 later devices descend from it; 6 cite it directly.
0 of 29 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
- K163361: ANTHEM™ Fracture System (2017), 14 descendants of its own
- K173166: ANTHEM Fracture System (2017), 11 descendants of its own
- K180554: ANTHEM Fracture System (2018), 10 descendants of its own
- K010545: TBW (2001), 10 descendants of its own
- K202496: ANTHEM Fracture System (2020), 8 descendants of its own

Source page: https://510kreport.com/device/K951303
Methodology: https://510kreport.com/methodology