The following data is part of a premarket notification filed by Bio-interfaces, Inc. with the FDA for Bii-pore(tm) Canal Wall Prosthesis.
Device ID | K934049 |
510k Number | K934049 |
Device Name: | BII-PORE(TM) CANAL WALL PROSTHESIS |
Classification | Bone Grafting Material, Synthetic |
Applicant | BIO-INTERFACES, INC. 11095 FLINTKOTE AVE. San Diego, CA 92121 |
Contact | John F Kay |
Correspondent | John F Kay BIO-INTERFACES, INC. 11095 FLINTKOTE AVE. San Diego, CA 92121 |
Product Code | LYC |
CFR Regulation Number | 872.3930 [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Traditional |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 1993-08-19 |
Decision Date | 1994-07-19 |