510(k) K223790 ยท PEK Spinous Process Plate
Huvex Interspinous Fusion System
| Applicant | Dio Medical Corp., East Norriton PA, US |
| Decision | Substantially Equivalent, Mar 9, 2023 |
| Received | Dec 19, 2022 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K223790
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.