510(k) K110733 ยท ODP Intervertebral Fusion Device With Bone Graft, Cervical
DAYTONA ANTERIOR CERVICAL CAGE
| Applicant | Spinenet, LLC, Round Rock TX, US |
| Decision | Substantially Equivalent, Aug 25, 2011 |
| Received | Mar 16, 2011 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K110733
| Date | Firm and product | Code | Linked 510(k) |
|---|---|---|---|
| Aug 27, 2013 | SpineNet SpineNet Anterior Cervical Cage, Lordotic, Peek (originally submitted as Daytona Anterior Cervical Cage)
Product Usage: Is indicated for use in skeletally mature patients with degenerative disc dise Terminated |
ODP | None listed |
Links come from the 510(k) numbers listed on each FDA recall record. We don't infer predicate chains.