FDA 510(k) Application Details - K171840

Device Classification Name	Drill, Surgical, Ent (Electric Or Pneumatic) Including Handpiece   More FDA Info for this Device
510(K) Number	K171840
Device Name	Drill, Surgical, Ent (Electric Or Pneumatic) Including Handpiece
Applicant	Stryker Corporation 4100 E. Milham Ave. Kalamazoo, MI 49001 US Other 510(k) Applications for this Company
Contact	Nicholas Werner Other 510(k) Applications for this Contact
Regulation Number	874.4250   More FDA Info for this Regulation Number
Classification Product Code	ERL Other 510(k) Applications for this Device   More FDA Info for this Product Code
Date Received	06/20/2017
Decision Date	09/15/2017
Decision	SESE - SUBST EQUIV
Classification Advisory Committee	EN - Ear, Nose, & Throat
Review Advisory Committee	EN - Ear, Nose, & Throat
Statement / Summary / Purged Status	Summary
Type	Traditional
Reviewed By Third Party	N
Expedited Review