K980463 is an FDA 510(k) clearance for the SPECTRUM DESIGNS CURVILINEAR CHIN IMPLANT. This device is classified as a Prosthesis, Chin, Internal (Class II - Special Controls, product code FWP).
Submitted by Spectrum Designs, Inc. (Goleta, US). The FDA issued a Cleared decision on May 6, 1998, 90 days after receiving the submission on February 5, 1998.
This device falls under the General & Plastic Surgery FDA review panel. Regulated under 21 CFR 878.3550.
| 510(k) Number | K980463 FDA.gov |
| FDA Decision | Cleared Substantially Equivalent - Traditional 510(k) (SESE) |
| Date Received | February 05, 1998 |
| Decision Date | May 06, 1998 |
| Days to Decision | 90 days |
| Submission Type | Traditional |
| Review Panel | General & Plastic Surgery (SU) |
| Summary | Summary PDF |
| Product Code | FWP — Prosthesis, Chin, Internal |
| Device Class | Class II - Special Controls |
| CFR Regulation | 21 CFR 878.3550 |