# K914812: K-Cap-E, Sterile

- Pathway: 510(k) (Traditional)
- Applicant: Westcon Orthopedics, Inc.
- Decided: Jan 9, 1992 after 76 days
- Product code: LYT (Fixation Accessory)
- Device class: 2
- Regulation: 21 CFR 888.3030
- Recalls of this device: none
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Lineage
No predicates in its family tree.
3 later devices descend from it; 1 cites it directly.
0 of 4 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
- K022597: K-FIX (2002), 2 descendants of its own
- K203698: CoLink Sfx Implant System (2021), 1 descendant of its own
- K231905: Electro-Spec Steri-Caps (2023), 0 descendants of its own

Source page: https://510kreport.com/device/K914812
Methodology: https://510kreport.com/methodology