The following data is part of a premarket notification filed by Applied Biomaterial Technologies with the FDA for Pec Implant.
Device ID | K913768 |
510k Number | K913768 |
Device Name: | PEC IMPLANT |
Classification | Implant, Muscle, Pectoralis |
Applicant | APPLIED BIOMATERIAL TECHNOLOGIES 3500 N.W. ANDERSON HILL RD. SUITE #101 SILVERDALE, WA 98383 |
Contact | GERALD L HANSON |
Correspondent | GERALD L HANSON APPLIED BIOMATERIAL TECHNOLOGIES 3500 N.W. ANDERSON HILL RD. SUITE #101 SILVERDALE, WA 98383 |
Product Code | MIC |
CFR Regulation Number | 874.3620 [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Traditional |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 1991-08-22 |
Decision Date | 1992-02-03 |