510(k) K231654 ยท NKG Posterior Cervical Screw System
NorthStar OCT System
| Applicant | Seaspine, Inc., Carlsbad CA, US |
| Decision | Substantially Equivalent, Aug 3, 2023 |
| Received | Jun 6, 2023 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K231654
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.