# K951302: Small Fragment Plates and Screws

- Pathway: 510(k) (Traditional)
- Applicant: Medpac
- Decided: May 5, 1995 after 44 days
- Product code: JDS (Nail, Fixation, Bone)
- Device class: 2
- Regulation: 21 CFR 888.3030
- Recalls of this device: 1 (0 Class I)
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Lineage
No predicates in its family tree.
7 later devices descend from it; 3 cite it directly.
0 of 8 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
- K222637: TriMed Wrist Fixation System 3 (2022), 3 descendants of its own
- K260390: Super Upper Limbs Versalock Plating System (2026), 1 descendant of its own
- K262537: Versalock Sterile Plating System (2026), 0 descendants of its own
- K251732: Wrist Fracture System (2026), 0 descendants of its own
- K254002: TriMed Volar Bearing Plates (VBEAL-13-7S); TriMed Volar Bearing Plates (VBEAR-13-7S); TriMed Volar Bearing Plates (VBEAL-14-7S); TriMed Volar Bearing Plates (VBEAR-14-7S); TriMed Volar Bearing Plates (VBEAL-16-7S); TriMed Volar Bearing Plates (VBEAR-16-7S) (2026), 0 descendants of its own

## Recalls of this device
- Aug 24, 2018 · Class II · Z-0118-2020: Modifications to the specification were not appropriately qualified through the company's design control process which may result in structural integrity issues of the device.

Source page: https://510kreport.com/device/K951302
Methodology: https://510kreport.com/methodology