The following data is part of a premarket notification filed by Collagen Matrix, Inc. with the FDA for Collagen Periodontal Membrane.
Device ID | K003339 |
510k Number | K003339 |
Device Name: | COLLAGEN PERIODONTAL MEMBRANE |
Classification | Barrier, Animal Source, Intraoral |
Applicant | COLLAGEN MATRIX, INC. 509 COMMERCE ST. Franklin Lakes,, NJ 07417 |
Contact | Shu-tung Li |
Correspondent | Shu-tung Li COLLAGEN MATRIX, INC. 509 COMMERCE ST. Franklin Lakes,, NJ 07417 |
Product Code | NPL |
CFR Regulation Number | 872.3930 [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Traditional |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 2000-10-25 |
Decision Date | 2001-01-08 |