510(k) K061353 ยท KWQ Appliance, Fixation, Spinal Intervertebral Body
TRINICA ANTERIOR LUMBAR PLATE SYSTEM
| Applicant | Zimmer Spine, Inc., Minneapolis MN, US |
| Decision | Substantially Equivalent, Aug 30, 2006 |
| Received | May 15, 2006 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K061353
| Date | Firm and product | Code | Linked 510(k) |
|---|---|---|---|
| Nov 18, 2013 | Zimmer, Inc. Trinica Anterior Lumbar Plate (ALP) system, part 07.01058.001. Non Sterile, Rx only. The Trinica Anterior Lumbar Plate System is a temporary supplemental fixation device consisting of a variety of sh Terminated |
KWQ | None listed |
Links come from the 510(k) numbers listed on each FDA recall record. We don't infer predicate chains.