BONE CEMENT RESTRICTOR— 510(k) K926216

Name: FDA 510(k) clearance K926216
Creator: U.S. Food and Drug Administration
Published: 1994-03-22

Substantially Equivalent

Biodynamic Technologies, Inc.

FDA 510(k) clearance K926216 for BONE CEMENT RESTRICTOR, Substantially Equivalent on 1994-03-22. Applicant: Biodynamic Technologies, Inc.. Device class: 2.

Clearance details

Applicant: Biodynamic Technologies, Inc.
Product code: Code JDK
Device class: Class 2
Regulation: 21 CFR 878.3300
Advisory panel: General, Plastic Surgery
Date received: 1992-12-10
Decision date: 1994-03-22
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Arlington, VA, US

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