510(k) K070341 ยท KWP Appliance, Fixation, Spinal Interlaminal
LDR SPINE EASYSPINE POSTERIOR OSTEOSYNTHESIS SYSTEM
| Applicant | Ldr Spine USA, Austin TX, US |
| Decision | Substantially Equivalent, Aug 8, 2007 |
| Received | Feb 6, 2007 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K070341
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.