510(k) K223770 ยท LFL Instrument, Ultrasonic Surgical
Sonopet 1Q 3 7cm 1Q Large
| Applicant | Stryker Corporation, Portage MI, US |
| Decision | Substantially Equivalent, Feb 16, 2023 |
| Received | Dec 15, 2022 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K223770
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.