K792352 is an FDA 510(k) clearance for the SYNTHES CERVICAL VERTABRAE PLATES. This device is classified as a Appliance, Fixation, Spinal Intervertebral Body (Class II - Special Controls, product code KWQ).
Submitted by DePuy Synthes (Raynham, US). The FDA issued a Cleared decision on December 6, 1979, 17 days after receiving the submission on November 19, 1979.
This device falls under the Orthopedic FDA review panel. Regulated under 21 CFR 888.3060.
| 510(k) Number | K792352 FDA.gov |
| FDA Decision | Cleared Substantially Equivalent - Traditional 510(k) (SESE) |
| Date Received | November 19, 1979 |
| Decision Date | December 06, 1979 |
| Days to Decision | 17 days |
| Submission Type | Traditional |
| Review Panel | Orthopedic (OR) |
| Summary | — |
| Product Code | KWQ — Appliance, Fixation, Spinal Intervertebral Body |
| Device Class | Class II - Special Controls |
| CFR Regulation | 21 CFR 888.3060 |