510(k) K020085 ยท MNH Orthosis, Spondylolisthesis Spinal Fixation
SINTEA BIOTECH POSTERIOR LUMBAR SYSTEM, MODEL PLS 00.T5.X
| Applicant | Sintea Biotech, Inc., Miami Beach FL, US |
| Decision | Substantially Equivalent, Dec 10, 2002 |
| Received | Jan 10, 2002 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K020085
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.