SYNOSS SYNTHETIC BONE GRAFT MATERIAL— 510(k) K072397

Name: FDA 510(k) clearance K072397
Creator: U.S. Food and Drug Administration
Published: 2007-10-18

Substantially Equivalent

Collagen Matrix, Inc.

FDA 510(k) clearance K072397 for SYNOSS SYNTHETIC BONE GRAFT MATERIAL, Substantially Equivalent on 2007-10-18. Applicant: Collagen Matrix, Inc.. Device class: 2.

Clearance details

Applicant: Collagen Matrix, Inc.
Product code: Code LYC
Device class: Class 2
Regulation: 21 CFR 872.3930
Advisory panel: Dental
Date received: 2007-08-27
Decision date: 2007-10-18
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Franklin Lakes, NJ, US

Download summary PDF View on FDA.gov ↗

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