FDA 510(k) Application Details - K043152

Device Classification Name	Orthosis, Spondyloisthesis Spinal Fixation   More FDA Info for this Device
510(K) Number	K043152
Device Name	Orthosis, Spondyloisthesis Spinal Fixation
Applicant	VERTEBRON, INC. 400 LONG BEACH BLVD. STRATFORD, CT 06615 US Other 510(k) Applications for this Company
Contact	LUIS NESPRIDO 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	11/15/2004
Decision Date	02/01/2005
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