510(k) K130548 ยท MAX Intervertebral Fusion Device With Bone Graft, Lumbar
EPICAGE INTERBODY FUSION DEVICE
| Applicant | Alphatec Spine, Inc., Carlsnad CA, US |
| Decision | Substantially Equivalent, Apr 18, 2013 |
| Received | Mar 4, 2013 |
| Type | Special |
| FDA record | Open on fda.gov |
Recalls that name K130548
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.