FDA 510(k) Application Details - K093670

Device Classification Name	Orthosis, Spondyloisthesis Spinal Fixation   More FDA Info for this Device
510(K) Number	K093670
Device Name	Orthosis, Spondyloisthesis Spinal Fixation
Applicant	STRYKER SPINE 2 PEARL COURT ALLENDALE, NJ 07401 US Other 510(k) Applications for this Company
Contact	PAULINE SHAND Other 510(k) Applications for this Contact
Regulation Number	888.3070   More FDA Info for this Regulation Number
Classification Product Code	MNH Other 510(k) Applications for this Device   More FDA Info for this Product Code
Date Received	11/27/2009
Decision Date	03/18/2010
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