MAESTRO CARPAL HEMIARTHROPLASTY— 510(k) K050028

Substantially Equivalent

Biomet Manufacturing, Inc.

FDA 510(k) clearance K050028 for MAESTRO CARPAL HEMIARTHROPLASTY, Substantially Equivalent on 2005-03-25. Applicant: Biomet Manufacturing, Inc..

Clearance details

Applicant: Biomet Manufacturing, Inc.
Product code: Code KWN
Advisory panel: Orthopedic
Date received: 2005-01-06
Decision date: 2005-03-25
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Warsaw, IN, US

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