FDA 510(k) Application Details - K122770

Device Classification Name	Plate, Fixation, Bone   More FDA Info for this Device
510(K) Number	K122770
Device Name	Plate, Fixation, Bone
Applicant	BIOMET MANUFACTURING CORP. 56 BELL DRIVE WARSAW, IN 46580 US Other 510(k) Applications for this Company
Contact	PATRICIA SANDBORN BERES 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	09/10/2012
Decision Date	03/28/2013
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