510(k) K073202 ยท MAX Intervertebral Fusion Device With Bone Graft, Lumbar
ARDIS SPACER
| Applicant | Abbott Spine, Inc., Austin TX, US |
| Decision | Substantially Equivalent, Jan 30, 2008 |
| Received | Nov 13, 2007 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K073202
| Date | Firm and product | Code | Linked 510(k) |
|---|---|---|---|
| Dec 22, 2012 | Zimmer, Inc. Zimmer Spine Ardis Inserter, Rx, non-sterile Terminated |
MAX | None listed |
Links come from the 510(k) numbers listed on each FDA recall record. We don't infer predicate chains.