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PhotoFix Decellularized Bovine Pericardium

K172085 Class II Traditional
Decision Date
2017-12-04
Sponsor / Applicant
Cryolife, Inc.

Technical Specification

510(k) Submission ID K172085
Product Code PSQ
Medical Specialty / Panel Cardiovascular
Regulation Citation 21 CFR 870.3470
Decision Date 2017-12-04
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

PhotoFix Decellularized Bovine Pericardium received FDA 510(k) clearance under submission number K172085, sponsored by Cryolife, Inc.. The device was reviewed via the Traditional premarket notification pathway and assigned to the Cardiovascular review panel. The statutory decision date of record is 2017-12-04.

Classification & Regulation

This clearance is catalogued under FDA product code PSQ and 21 CFR 870.3470, within the Cardiovascular review panel as a Class II device.