# K955553: Perfecta Revision Hip System

- Pathway: 510(k) (Traditional)
- Applicant: Wrightmedicaltechnologyinc
- Decided: Oct 24, 1996 after 324 days
- Product code: LWJ (Prosthesis, Hip, Semi-Constrained, Metal/Polymer, Uncemented)
- Device class: 2
- Regulation: 21 CFR 888.3360
- 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) PERFECTA® Hip System by Orthomet, a division of Wright Medical Technology, Inc.: named in the summary without a submission number
- (no number) Osteonics® Arc Depositioned Femoral Components: named in the summary without a submission number

## Indications for use
The PERFECTA® Revision Hip System is intended to be used in total hip arthroplasty for reduction or relief of pain and/or improved hip function in skeletally mature patients.

Source page: https://510kreport.com/device/K955553
Methodology: https://510kreport.com/methodology