FDA 510(k) Application Details - K973098

Device Classification Name	Cerclage, Fixation   More FDA Info for this Device
510(K) Number	K973098
Device Name	Cerclage, Fixation
Applicant	PLUS ORTHOPEDICS 835 CORTEZ LN. FOREST CITY, CA 94404 US Other 510(k) Applications for this Company
Contact	HARTMUT LOCH Other 510(k) Applications for this Contact
Regulation Number	888.3010   More FDA Info for this Regulation Number
Classification Product Code	JDQ Other 510(k) Applications for this Device   More FDA Info for this Product Code
Date Received	08/19/1997
Decision Date	10/27/1997
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