PROSTHETIC CEMENT REMOVER— 510(k) K904180

Name: FDA 510(k) clearance K904180
Creator: U.S. Food and Drug Administration
Published: 1990-11-20

Substantially Equivalent

Origin Medsystems, Inc.

FDA 510(k) clearance K904180 for PROSTHETIC CEMENT REMOVER, Substantially Equivalent on 1990-11-20. Applicant: Origin Medsystems, Inc.. Device class: 2.

Clearance details

Applicant: Origin Medsystems, Inc.
Product code: Code LZV
Device class: Class 2
Regulation: 21 CFR 888.4580
Advisory panel: Orthopedic
Date received: 1990-09-11
Decision date: 1990-11-20
Decision: Substantially Equivalent
Clearance type: Traditional
Location: San Mateo, CA, US

Download summary PDF View on FDA.gov ↗

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