# K951304: Synthes 2.7 MM Cannulated Screw and Threaded Washer

- Pathway: 510(k) (Traditional)
- Applicant: Synthes (Usa)
- Decided: Jun 16, 1995 after 86 days
- Product code: HWC (Screw, Fixation, Bone)
- Device class: 2
- Regulation: 21 CFR 888.3040
- 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.
2 later devices descend from it; 1 cites it directly.
0 of 3 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
- K191118: Avanti Distal Radius and Forearm System (2019), 1 descendant of its own
- K261145: Avanti Distal Elbow ORIF System (2026), 0 descendants of its own

## Recalls of this device
- Jun 30, 2014 · Class II · Z-2265-2014: A screw set was returned from the field for destruction after being exposed to flood water, which was erroneously reprocessed and returned to the field. Initial investigative testing indicated the com

Source page: https://510kreport.com/device/K951304
Methodology: https://510kreport.com/methodology