510(k) K201755 ยท MAX Intervertebral Fusion Device With Bone Graft, Lumbar
WaveForm L Interbody System, WaveForm TO Interbody System, WaveForm TA Interbody System
| Applicant | SeaSpine Orthopedics Corporation, Carlsbad CA, US |
| Decision | Substantially Equivalent, Dec 15, 2020 |
| Received | Jun 29, 2020 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K201755
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.