510(k) K102449 ยท ODP Intervertebral Fusion Device With Bone Graft, Cervical
BRIGHT SPINE GALILEO SPINAL SPACER SYSTEM
| Applicant | Bright Spine, Inc., Boca Raton FL, US |
| Decision | Substantially Equivalent, Feb 11, 2011 |
| Received | Aug 27, 2010 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K102449
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.