510(k) K031823 ยท MQP Spinal Vertebral Body Replacement Device
HEDROCEL VERTEBRAL BODY REPLACEMENT, MODEL 06-172-00XX1
| Applicant | Implex Corp., Allendale NJ, US |
| Decision | Substantially Equivalent, Jul 11, 2003 |
| Received | Jun 13, 2003 |
| Type | Special |
| FDA record | Open on fda.gov |
Recalls that name K031823
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.