510(k) K180230 ยท MAX Intervertebral Fusion Device With Bone Graft, Lumbar
NEST Interbody System
| Applicant | Paonan Biotech Co., Ltd., Taipei City 114, TW |
| Decision | Substantially Equivalent, Jan 25, 2019 |
| Received | Jan 26, 2018 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K180230
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.