The following data is part of a premarket notification filed by Byron Medical with the FDA for Byron Silicone Chin Implants.
| Device ID | K863397 |
| 510k Number | K863397 |
| Device Name: | BYRON SILICONE CHIN IMPLANTS |
| Classification | Prosthesis, Chin, Internal |
| Applicant | BYRON MEDICAL 3280 E. HEMISPHERE LOOP SUITE 100 Tucson, AZ 85706 |
| Contact | Byron Economidy |
| Correspondent | Byron Economidy BYRON MEDICAL 3280 E. HEMISPHERE LOOP SUITE 100 Tucson, AZ 85706 |
| Product Code | FWP |
| CFR Regulation Number | 878.3550 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 1986-09-03 |
| Decision Date | 1986-09-18 |