510(k) K191625 ยท JWH Prosthesis, Knee, Patellofemorotibial, Semi-Constrained, Cemented, Polymer/Metal/Polymer
Persona Revision Knee System
| Applicant | Zimmer, Inc., Warsaw IN, US |
| Decision | Substantially Equivalent, Sep 5, 2019 |
| Received | Jun 18, 2019 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K191625
| Date | Firm and product | Code | Linked 510(k) |
|---|---|---|---|
| Jun 24, 2026 | Zimmer, Inc. Brand Name: Persona Revision
Product Name: Persona Revision Trabecular Metal Femoral Distal Augment
Model/Catalog Number: 42-5572-066-10
Software Version: N/A
Product Description: Persona Revision Tra Open, Classified |
MBH | None listed |
Links come from the 510(k) numbers listed on each FDA recall record. We don't infer predicate chains.