510(k) K190963 ยท HRS Plate, Fixation, Bone
DePuy Synthes Craniomaxillofacial Sternal Devices - MR Conditional
| Applicant | Synthes (USA) Products, LLC, West Chester PA, US |
| Decision | Substantially Equivalent, Jul 23, 2019 |
| Received | Apr 12, 2019 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K190963
No recall in the FDA data names this 510(k).
Links come from the 510(k) numbers listed on each FDA recall record. We don't infer predicate chains.