FDA 510(k) Application Details - K133460

Device Classification Name	Screw, Fixation, Bone   More FDA Info for this Device
510(K) Number	K133460
Device Name	Screw, Fixation, Bone
Applicant	MEDARTIS AG 12264 EL CAMINO REAL, STE 400 SAN DIEGO, CA 92130 US Other 510(k) Applications for this Company
Contact	ALLISON KOMIYAMA Other 510(k) Applications for this Contact
Regulation Number	888.3040   More FDA Info for this Regulation Number
Classification Product Code	HWC Other 510(k) Applications for this Device   More FDA Info for this Product Code
Date Received	11/12/2013
Decision Date	12/18/2013
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