510(k) K182339 · NKB Thoracolumbosacral Pedicle Screw System
LEUCADIA AUTOLOK Pedicle Screw System
| Applicant | Clearview Orthopedic Development, LLC, Irvine CA, US |
| Decision | Substantially Equivalent, Dec 12, 2018 |
| Received | Aug 28, 2018 |
| Type | Special |
| FDA record | Open on fda.gov |
Recalls that name K182339
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.