510(k) K173521 ยท KWQ Appliance, Fixation, Spinal Intervertebral Body
SeaSpine Cabo ACP (Anterior Cervical Plate) System
| Applicant | SeaSpine Orthopedics Corporation, Carlsbad CA, US |
| Decision | Substantially Equivalent, Jan 24, 2018 |
| Received | Nov 14, 2017 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K173521
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.