FDA 510(k) Application Details - K151813

Device Classification Name	Orthosis, Spinal Pedicle Fixation   More FDA Info for this Device
510(K) Number	K151813
Device Name	Orthosis, Spinal Pedicle Fixation
Applicant	SPINE WAVE, INC. 3 ENTERPRISE DRIVE, SUITE 210 SHELTON, CT 06484 US Other 510(k) Applications for this Company
Contact	Ronald K Smith Other 510(k) Applications for this Contact
Regulation Number	888.3070   More FDA Info for this Regulation Number
Classification Product Code	MNI Other 510(k) Applications for this Device   More FDA Info for this Product Code
Date Received	07/02/2015
Decision Date	07/31/2015
Decision	SESE - SUBST EQUIV
Classification Advisory Committee	OR - Orthopedic
Review Advisory Committee	OR - Orthopedic
Statement / Summary / Purged Status	Summary
Type	Special
Reviewed By Third Party	N
Expedited Review