CEMENTRALIZER DISTAL STEM CENTRALIZER— 510(k) K951930

Name: FDA 510(k) clearance K951930
Creator: U.S. Food and Drug Administration
Published: 1995-07-11

Substantially Equivalent

Depuy, Inc.

FDA 510(k) clearance K951930 for CEMENTRALIZER DISTAL STEM CENTRALIZER, Substantially Equivalent on 1995-07-11. Applicant: Depuy, Inc.. Device class: 2.

Clearance details

Applicant: Depuy, Inc.
Product code: Code LZN
Device class: Class 2
Regulation: 21 CFR 878.3300
Advisory panel: General, Plastic Surgery
Date received: 1995-04-05
Decision date: 1995-07-11
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Warsaw, IN, US

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