MICROVASCULAR ANASTOMOTIC DEVICE— 510(k) K040163

Name: FDA 510(k) clearance K040163
Creator: U.S. Food and Drug Administration
Published: 2004-04-16

Substantially Equivalent

Synovis Micro Companies Alliance, Inc.

FDA 510(k) clearance K040163 for MICROVASCULAR ANASTOMOTIC DEVICE, Substantially Equivalent on 2004-04-16. Applicant: Synovis Micro Companies Alliance, Inc.. Device class: 2.

Clearance details

Applicant: Synovis Micro Companies Alliance, Inc.
Product code: Code MVR
Device class: Class 2
Regulation: 21 CFR 878.4300
Advisory panel: General, Plastic Surgery
Date received: 2004-01-26
Decision date: 2004-04-16
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Birmingham, AL, US

Download summary PDF View on FDA.gov ↗

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Data sourced from openFDA. This site is unofficial and independent of the FDA.