RABEA CEMENT RESTRICTOR— 510(k) K020836

Substantially Equivalent

Signus Medical, LLC

FDA 510(k) clearance K020836 for RABEA CEMENT RESTRICTOR, Substantially Equivalent on 2002-06-11. Applicant: Signus Medical, LLC. Device class: 2.

Clearance details

Applicant: Signus Medical, LLC
Product code: Product code JDK
Device class: Class 2
Regulation: 21 CFR 878.3300
Advisory panel: General, Plastic Surgery
Date received: 2002-03-14
Decision date: 2002-06-11
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Minneapolis, MN, US

Download summary PDF View on FDA.gov ↗

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Data sourced from openFDA. This site is unofficial and independent of the FDA.