MOTECH TITANIUM SURGICAL MESH— 510(k) K900138

Name: FDA 510(k) clearance K900138
Creator: U.S. Food and Drug Administration
Published: 1990-03-20

Substantially Equivalent

Biedermann Motech GmbH

FDA 510(k) clearance K900138 for MOTECH TITANIUM SURGICAL MESH, Substantially Equivalent on 1990-03-20. Applicant: Biedermann Motech GmbH. Device class: 2.

Clearance details

Applicant: Biedermann Motech GmbH
Product code: Code EZX
Device class: Class 2
Regulation: 21 CFR 878.3300
Advisory panel: General, Plastic Surgery
Date received: 1990-01-11
Decision date: 1990-03-20
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Olney, MD, US

Download summary PDF View on FDA.gov ↗

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