The following data is part of a premarket notification filed by Cook Biotech, Inc. with the FDA for Ss Matrix.
| Device ID | K020732 |
| 510k Number | K020732 |
| Device Name: | SS MATRIX |
| Classification | Dressing, Wound, Collagen |
| Applicant | COOK BIOTECH, INC. 3055 KENT AVE. West Lafayette, IN 47906 -1076 |
| Contact | Mark Bleyer |
| Correspondent | Mark Bleyer COOK BIOTECH, INC. 3055 KENT AVE. West Lafayette, IN 47906 -1076 |
| Product Code | KGN |
| CFR Regulation Number | 510(k) Premarket Notification [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 2002-03-06 |
| Decision Date | 2002-05-30 |
| Summary: | summary |