VERITAS COLLAGEN MATRIX— 510(k) K030879

Name: FDA 510(k) clearance K030879
Creator: U.S. Food and Drug Administration
Published: 2003-04-24

Substantially Equivalent

Synovis Surgical Innovations

FDA 510(k) clearance K030879 for VERITAS COLLAGEN MATRIX, Substantially Equivalent on 2003-04-24. Applicant: Synovis Surgical Innovations. Device class: 2.

Clearance details

Applicant: Synovis Surgical Innovations
Product code: Code OXE
Device class: Class 2
Regulation: 21 CFR 878.3300
Advisory panel: General, Plastic Surgery
Date received: 2003-03-20
Decision date: 2003-04-24
Decision: Substantially Equivalent
Clearance type: Traditional
Location: St. Paul, MN, US

Download summary PDF View on FDA.gov ↗

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