510(k) K081673 ยท MAX Intervertebral Fusion Device With Bone Graft, Lumbar
DYN-ALIF ANTEROLATERAL INTERVERTEBRAL BODY FUSION DEVICE
| Applicant | Ionics Medical Corp., Ether NC, US |
| Decision | Substantially Equivalent, Nov 14, 2008 |
| Received | Jun 13, 2008 |
| Type | Abbreviated |
| FDA record | Open on fda.gov |
Recalls that name K081673
No recall in the FDA data names this 510(k).
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