510(k) K130630 ยท MAX Intervertebral Fusion Device With Bone Graft, Lumbar
PLATEAU SPACER SYSTEM TITANIUM
| Applicant | Life Spine, Inc., Hoffman Estates IL, US |
| Decision | Substantially Equivalent, Jun 13, 2013 |
| Received | Mar 8, 2013 |
| Type | Special |
| FDA record | Open on fda.gov |
Recalls that name K130630
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.