510(k) K102026 ยท MAX Intervertebral Fusion Device With Bone Graft, Lumbar
SEASPINE SPACER SYSTEM
| Applicant | Seaspine, Inc., Vista CA, US |
| Decision | Substantially Equivalent, May 12, 2011 |
| Received | Jul 19, 2010 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K102026
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.