FDA 510(k) Application Details - K151974

Device Classification Name	Orthosis, Spinal Pedicle Fixation, For Degenerative Disc Disease   More FDA Info for this Device
510(K) Number	K151974
Device Name	Orthosis, Spinal Pedicle Fixation, For Degenerative Disc Disease
Applicant	BIOMET SPINE 310 INTERLOCKEN PARKWAY, SUITE 120 BROOMFIELD, CO 80021 US Other 510(k) Applications for this Company
Contact	ALEXANDRA BECK Other 510(k) Applications for this Contact
Regulation Number	888.3070   More FDA Info for this Regulation Number
Classification Product Code	NKB Other 510(k) Applications for this Device   More FDA Info for this Product Code
Date Received	07/16/2015
Decision Date	11/13/2015
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