EXETER INTRAMEDULLARY BONE PLUG— 510(k) K933077

Name: FDA 510(k) clearance K933077
Creator: U.S. Food and Drug Administration
Published: 1995-05-16

Substantially Equivalent for Some Indications

Howmedica Corp.

FDA 510(k) clearance K933077 for EXETER INTRAMEDULLARY BONE PLUG, Substantially Equivalent for Some Indications on 1995-05-16. Applicant: Howmedica Corp.. Device class: 2.

Clearance details

Applicant: Howmedica Corp.
Product code: Code LZN
Device class: Class 2
Regulation: 21 CFR 878.3300
Advisory panel: General, Plastic Surgery
Date received: 1993-06-23
Decision date: 1995-05-16
Decision: Substantially Equivalent for Some Indications
Clearance type: Traditional
Location: Rutherford, NJ, US

Download summary PDF View on FDA.gov ↗

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