510(k) K100305 ยท MAX Intervertebral Fusion Device With Bone Graft, Lumbar
ETURN SPINAL IMPLANT MODEL ETURN XX-12; ETURN XX-16 WHERE XX=07, 09, 11, 13, OR 15 AND ETURN XX-12 K; ETURN XX-16 K WHER
| Applicant | Icotec, Minneapolis MN, US |
| Decision | Substantially Equivalent, Jul 21, 2011 |
| Received | Feb 3, 2010 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K100305
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.