510(k) K041989 ยท KWQ Appliance, Fixation, Spinal Intervertebral Body
SINTEA BIOTECH ANTERIOR PLATE SYSTEM, MODEL ACP.XX.T5.X
| Applicant | Sintea Biotech, Inc., Miami Beach FL, US |
| Decision | Substantially Equivalent, Sep 16, 2004 |
| Received | Jul 23, 2004 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K041989
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.