OSTEOSET DBM PELLETS— 510(k) K053642

Name: FDA 510(k) clearance K053642
Creator: U.S. Food and Drug Administration
Published: 2006-01-26

Substantially Equivalent

Wrightmedicaltechnologyinc

FDA 510(k) clearance K053642 for OSTEOSET DBM PELLETS, Substantially Equivalent on 2006-01-26. Applicant: Wrightmedicaltechnologyinc. Device class: 2.

Clearance details

Applicant: Wrightmedicaltechnologyinc
Product code: Code MBP
Device class: Class 2
Regulation: 21 CFR 888.3045
Advisory panel: Orthopedic
Date received: 2005-12-30
Decision date: 2006-01-26
Decision: Substantially Equivalent
Clearance type: Special
Location: Arlington, TN, US

Download summary PDF View on FDA.gov ↗

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