CEMENT RESTRICTOR FOR PROFORMA AND PERFECTA TOTAL— 510(k) K923909

Name: FDA 510(k) clearance K923909
Creator: U.S. Food and Drug Administration
Published: 1992-11-04

Substantially Equivalent

Orthomet, Inc.

FDA 510(k) clearance K923909 for CEMENT RESTRICTOR FOR PROFORMA AND PERFECTA TOTAL, Substantially Equivalent on 1992-11-04. Applicant: Orthomet, Inc.. Device class: 2.

Clearance details

Applicant: Orthomet, Inc.
Product code: Code LZN
Device class: Class 2
Regulation: 21 CFR 878.3300
Advisory panel: General, Plastic Surgery
Date received: 1992-08-04
Decision date: 1992-11-04
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Minneapolis, MN, US

Download summary PDF View on FDA.gov ↗

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