FDA 510(k) Application Details - K100805

Device Classification Name	Orthosis, Spine, Plate, Laminoplasty, Metal   More FDA Info for this Device
510(K) Number	K100805
Device Name	Orthosis, Spine, Plate, Laminoplasty, Metal
Applicant	BIOMET SPINE (AKA EBI, LLC) 100 INTERPACE PARKWAY PARSIPPANY, NJ 07054 US Other 510(k) Applications for this Company
Contact	SHIKHA GOLA Other 510(k) Applications for this Contact
Regulation Number	888.3050   More FDA Info for this Regulation Number
Classification Product Code	NQW Other 510(k) Applications for this Device   More FDA Info for this Product Code
Date Received	03/22/2010
Decision Date	07/20/2010
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