FDA 510(k) Application Details - K172709

Device Classification Name	Drills, Burrs, Trephines & Accessories (Simple, Powered)   More FDA Info for this Device
510(K) Number	K172709
Device Name	Drills, Burrs, Trephines & Accessories (Simple, Powered)
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	882.4310   More FDA Info for this Regulation Number
Classification Product Code	HBE Other 510(k) Applications for this Device   More FDA Info for this Product Code
Date Received	09/08/2017
Decision Date	10/17/2018
Decision	SESE - SUBST EQUIV
Classification Advisory Committee	NE - Neurology
Review Advisory Committee	NE - Neurology
Statement / Summary / Purged Status	Summary
Type	Traditional
Reviewed By Third Party	N
Expedited Review