FDA 510(k) Application Details - K151865

Device Classification Name	Patch, Pledget And Intracardiac, Petp, Ptfe, Polypropylene   More FDA Info for this Device
510(K) Number	K151865
Device Name	Patch, Pledget And Intracardiac, Petp, Ptfe, Polypropylene
Applicant	AESCULAP, INC. 3773 CORPORATE PARKWAY CENTER VALLEY, PA 18034 US Other 510(k) Applications for this Company
Contact	KATHY A. RACOSKY Other 510(k) Applications for this Contact
Regulation Number	870.3470   More FDA Info for this Regulation Number
Classification Product Code	DXZ Other 510(k) Applications for this Device   More FDA Info for this Product Code
Date Received	07/08/2015
Decision Date	10/27/2015
Decision	SESE - SUBST EQUIV
Classification Advisory Committee	CV - Cardiovascular
Review Advisory Committee	CV - Cardiovascular
Statement / Summary / Purged Status	Summary
Type	Traditional
Reviewed By Third Party	N
Expedited Review