510(k) K102121 ยท OVD Intervertebral Fusion Device With Integrated Fixation, Lumbar
ECLIPSE VERTEBRAL SPACER SYSTEM-LUMBAR
| Applicant | Apollo Spine, Inc., Stoughton MA, US |
| Decision | Substantially Equivalent, Jan 12, 2011 |
| Received | Jul 29, 2010 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K102121
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.