FDA 510(k) Application Details - K152781

Device Classification Name	Orthosis, Spinal Pedicle Fixation, For Degenerative Disc Disease   More FDA Info for this Device
510(K) Number	K152781
Device Name	Orthosis, Spinal Pedicle Fixation, For Degenerative Disc Disease
Applicant	SHANGHAI SANYOU MEDICAL CO, LTD 1988 JIATANG ROAD JIADIANG DISTRICT 201807 CN Other 510(k) Applications for this Company
Contact	DAVID FAN 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	09/25/2015
Decision Date	02/12/2016
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