PFC CEMENT RESTRICTOR— 510(k) K951934

Name: FDA 510(k) clearance K951934
Creator: U.S. Food and Drug Administration
Published: 1995-05-16

Substantially Equivalent for Some Indications

Johnson & Johnson Professionals, Inc.

FDA 510(k) clearance K951934 for PFC CEMENT RESTRICTOR, Substantially Equivalent for Some Indications on 1995-05-16. Applicant: Johnson & Johnson Professionals, Inc.. Device class: 2.

Clearance details

Applicant: Johnson & Johnson Professionals, Inc.
Product code: Code LZN
Device class: Class 2
Regulation: 21 CFR 878.3300
Advisory panel: General, Plastic Surgery
Date received: 1995-04-25
Decision date: 1995-05-16
Decision: Substantially Equivalent for Some Indications
Clearance type: Traditional
Location: Raritan, NJ, US

Download summary PDF View on FDA.gov ↗

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