510(k) K220319 ยท HWC Screw, Fixation, Bone
Asnis III Cannulated Screw System, Asnis PRO Cannulated Screw System
| Applicant | Stryker GmbH, Mahwah NJ, US |
| Decision | Substantially Equivalent, Jun 10, 2022 |
| Received | Feb 3, 2022 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K220319
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.