FDA 510(k) Application Details - K092528

Device Classification Name	Plate, Fixation, Bone   More FDA Info for this Device
510(K) Number	K092528
Device Name	Plate, Fixation, Bone
Applicant	BIOMET TRAUMA (AKA EBI, LP) 100 INTERPACE PARKWAY PARSIPPANY, NJ 07054 US Other 510(k) Applications for this Company
Contact	MARGARET CROWE Other 510(k) Applications for this Contact
Regulation Number	888.3030   More FDA Info for this Regulation Number
Classification Product Code	HRS Other 510(k) Applications for this Device   More FDA Info for this Product Code
Date Received	08/18/2009
Decision Date	05/21/2010
Decision	SESE - SUBST EQUIV
Classification Advisory Committee	OR - Orthopedic
Review Advisory Committee	OR - Orthopedic
Statement / Summary / Purged Status	Summary
Type	Traditional
Reviewed By Third Party	N
Expedited Review