510(k) K153629 ยท OVE Intervertebral Fusion Device With Integrated Fixation, Cervical
ArcadiusXP C Spinal System
| Applicant | Aesculap Implant Systems, Inc., Center Valley PA, US |
| Decision | Substantially Equivalent, May 25, 2016 |
| Received | Dec 18, 2015 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K153629
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.