FDA 510(k) Application Details - K963367

Device Classification Name	Pin, Fixation, Smooth   More FDA Info for this Device
510(K) Number	K963367
Device Name	Pin, Fixation, Smooth
Applicant	RMS DIV. 8600 EVERGREEN BLVD. MINNEAPOLIS, MN 55433-6036 US Other 510(k) Applications for this Company
Contact	JODI LOCHER Other 510(k) Applications for this Contact
Regulation Number	888.3040   More FDA Info for this Regulation Number
Classification Product Code	HTY Other 510(k) Applications for this Device   More FDA Info for this Product Code
Date Received	08/27/1996
Decision Date	10/30/1996
Decision	SESE - SUBST EQUIV
Classification Advisory Committee	OR - Orthopedic
Review Advisory Committee	OR - Orthopedic
Statement / Summary / Purged Status	Statement
Type	Traditional
Reviewed By Third Party	N
Expedited Review