MODIFICATION TO SYMPHONY GRAFT DELIVERY SYSTEM— 510(k) K010320

Name: FDA 510(k) clearance K010320
Creator: U.S. Food and Drug Administration
Published: 2001-03-01

Substantially Equivalent

Depuyacromed

FDA 510(k) clearance K010320 for MODIFICATION TO SYMPHONY GRAFT DELIVERY SYSTEM, Substantially Equivalent on 2001-03-01. Applicant: Depuyacromed. Device class: 2.

Clearance details

Applicant: Depuyacromed
Product code: Code LYC
Device class: Class 2
Regulation: 21 CFR 872.3930
Advisory panel: Dental
Date received: 2001-02-02
Decision date: 2001-03-01
Decision: Substantially Equivalent
Clearance type: Special
Location: Raynham, MA, US

Download summary PDF View on FDA.gov ↗

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