TROCHANTER MESH— 510(k) K945027

Name: FDA 510(k) clearance K945027
Creator: U.S. Food and Drug Administration
Published: 1995-02-01

Substantially Equivalent for Some Indications

Acu Med, Inc.

FDA 510(k) clearance K945027 for TROCHANTER MESH, Substantially Equivalent for Some Indications on 1995-02-01. Applicant: Acu Med, Inc.. Device class: 2.

Clearance details

Applicant: Acu Med, Inc.
Product code: Code EZX
Device class: Class 2
Regulation: 21 CFR 878.3300
Advisory panel: General, Plastic Surgery
Date received: 1994-10-13
Decision date: 1995-02-01
Decision: Substantially Equivalent for Some Indications
Clearance type: Traditional
Location: Beaverton, OR, US

Download summary PDF View on FDA.gov ↗

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