# K955837: Cannulated Plus Hip Screw (Sterile)

- Pathway: 510(k) (Traditional)
- Applicant: Wrightmedicaltechnologyinc
- Decided: Mar 4, 1996 after 69 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.
No later device cites it as a predicate yet.
0 of 1 device in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- None. The FDA summary names its predicate without a number.
- (no number) Cannulated PLUS™ Hip Screw: named in the summary without a submission number

## Indications for use
The Cannulated PLUS™ Hip Screw (Sterile) is intended to be used in the fixation of cancellous bone, for treatment of conditions such as, but not limited to: femoral neck fractures; arthrodesis of the hip; femoral condyle fractures; tibial plateau fractures; ankle malleolar fractures; or elbow fractures

Source page: https://510kreport.com/device/K955837
Methodology: https://510kreport.com/methodology