INTERBODY INNOVATIONS CEMENT RESTRICTOR— 510(k) K051371

Name: FDA 510(k) clearance K051371
Creator: U.S. Food and Drug Administration
Published: 2005-12-06

Unknown

Interbody Innovations, Llp

FDA 510(k) clearance K051371 for INTERBODY INNOVATIONS CEMENT RESTRICTOR, Unknown on 2005-12-06. Applicant: Interbody Innovations, Llp. Device class: 2.

Clearance details

Applicant: Interbody Innovations, Llp
Product code: Code JDK
Device class: Class 2
Regulation: 21 CFR 878.3300
Advisory panel: General, Plastic Surgery
Date received: 2005-05-26
Decision date: 2005-12-06
Decision: Unknown
Clearance type: Traditional
Location: Clearwater, FL, US

Download summary PDF View on FDA.gov ↗

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