FDA 510(k) Application Details - K123717

Device Classification Name	Orthosis, Spinal Pedicle Fixation, For Degenerative Disc Disease   More FDA Info for this Device
510(K) Number	K123717
Device Name	Orthosis, Spinal Pedicle Fixation, For Degenerative Disc Disease
Applicant	ULRICH GMBH & CO. KG 612 TRADE CENTER BLVD CHESTERFIELD, MO 63005 US Other 510(k) Applications for this Company
Contact	HANS STOVER 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	12/04/2012
Decision Date	03/04/2013
Decision	SESU - SE - WITH LIMITATIONS
Classification Advisory Committee	OR - Orthopedic
Review Advisory Committee	OR - Orthopedic
Statement / Summary / Purged Status	Summary
Type	Traditional
Reviewed By Third Party	N
Expedited Review