510(k) K103033 ยท ODP Intervertebral Fusion Device With Bone Graft, Cervical
TRABECULAR METAL FUSION DEVICE MODEL 06-101-XXXXX, 06-102-XXXXX AND 08-100-XXXXX
| Applicant | Zimmer Trabecular Metal Technology, Parsippany NJ, US |
| Decision | Substantially Equivalent, Jan 10, 2011 |
| Received | Oct 13, 2010 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K103033
No recall in the FDA data names this 510(k).
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