FDA 510(k) Application Details - K140400

Device Classification Name	Stimulator, Nerve   More FDA Info for this Device
510(K) Number	K140400
Device Name	Stimulator, Nerve
Applicant	STRYKER CORPORATION 2 PEARL COURT ALLENDALE, NJ 07401 US Other 510(k) Applications for this Company
Contact	SORAYA KING Other 510(k) Applications for this Contact
Regulation Number	874.1820   More FDA Info for this Regulation Number
Classification Product Code	ETN Other 510(k) Applications for this Device   More FDA Info for this Product Code
Date Received	02/18/2014
Decision Date	07/01/2014
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