510(k) K142579 ยท HRS Plate, Fixation, Bone
Zimmer Periarticular Plating System
| Applicant | Zimmer, Inc., Warsaw IN, US |
| Decision | Substantially Equivalent, Oct 22, 2014 |
| Received | Sep 15, 2014 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K142579
| Date | Firm and product | Code | Linked 510(k) |
|---|---|---|---|
| Oct 10, 2019 | Zimmer Biomet, Inc. Periarticular Plates - Tibial, Item Nos. 00234700304
00234700306
00234700308
00234700310
00234700312
00234700314
00234700316
00234700404
00234700406
00234700408
00234700410
00234700412
00234700414
002 Terminated |
HRS | None listed |
| Oct 10, 2019 | Zimmer Biomet, Inc. PERI DIST VOLAR/DORSAL T/DORSAL DELTA RADIAL, Item Nos.
00234801303
00234801304
00234801306
00234801308
00234801310
00234801312
00234801403
00234801404
00234801406
00234801408
00234801410
00234801412 Terminated |
HRS | None listed |
Links come from the 510(k) numbers listed on each FDA recall record. We don't infer predicate chains.