The following data is part of a premarket notification filed by Cryolife, Inc. with the FDA for Photofix Decellularized Bovine Pericardium.
Device ID | K172085 |
510k Number | K172085 |
Device Name: | PhotoFix Decellularized Bovine Pericardium |
Classification | Intracardiac Patch Or Pledget, Biologically Derived |
Applicant | CryoLife, Inc. 1655 Roberts Blvd. NW Kennesaw, GA 30144 |
Contact | Heather Emerick |
Correspondent | Heather Emerick CryoLife, Inc. 1655 Roberts Blvd. NW Kennesaw, GA 30144 |
Product Code | PSQ |
CFR Regulation Number | 870.3470 [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Traditional |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 2017-07-11 |
Decision Date | 2017-12-04 |
Summary: | summary |