510(k) K220261 ยท ODP Intervertebral Fusion Device With Bone Graft, Cervical
NEST-C Interbody System
| Applicant | Paonan Biotech Co., Ltd., Taipei City, TW |
| Decision | Substantially Equivalent, Apr 24, 2023 |
| Received | Jan 31, 2022 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K220261
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.