SKELITE RESORBABLE CEMENT RESTRICTOR— 510(k) K051836

Unknown

Millenium Biologix, Inc.

FDA 510(k) clearance K051836 for SKELITE RESORBABLE CEMENT RESTRICTOR, Unknown on 2005-11-21. Applicant: Millenium Biologix, Inc.. Device class: 2.

Clearance details

Applicant: Millenium Biologix, Inc.
Product code: Code JDK
Device class: Class 2
Regulation: 21 CFR 878.3300
Advisory panel: General, Plastic Surgery
Date received: 2005-07-06
Decision date: 2005-11-21
Decision: Unknown
Clearance type: Traditional
Location: West Cadwell, NJ, 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.