FDA 510(k) Application Details - K970829

Device Classification Name	Screw, Fixation, Bone   More FDA Info for this Device
510(K) Number	K970829
Device Name	Screw, Fixation, Bone
Applicant	TORNIER 1000 BURNETT AVE. SUITE 450 CONCORD, CA 94520 US Other 510(k) Applications for this Company
Contact	DAVID W SCHLERF 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	03/06/1997
Decision Date	12/22/1998
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