FDA 510(k) Application Details - K151888

Device Classification Name	Cerclage, Fixation   More FDA Info for this Device
510(K) Number	K151888
Device Name	Cerclage, Fixation
Applicant	FRONTIER MEDICAL DEVICES, INC. 512 FOURTH STREET GWINN, MI 49841 US Other 510(k) Applications for this Company
Contact	BETHANY BYMAN 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	07/10/2015
Decision Date	10/30/2015
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