FDA 510(k) Application Details - K203807

Device Classification Name	Hearing Aid, Bone Conduction, Implanted   More FDA Info for this Device
510(K) Number	K203807
Device Name	Hearing Aid, Bone Conduction, Implanted
Applicant	Oticon Medical AB Datavagen 37B Askim SE-436 32 SE Other 510(k) Applications for this Company
Contact	Carolina Anker Wessling Other 510(k) Applications for this Contact
Regulation Number	874.3300   More FDA Info for this Regulation Number
Classification Product Code	MAH Other 510(k) Applications for this Device   More FDA Info for this Product Code
Date Received	12/28/2020
Decision Date	03/03/2021
Decision	SESE - SUBST EQUIV
Classification Advisory Committee	EN - Ear, Nose, & Throat
Review Advisory Committee	EN - Ear, Nose, & Throat
Statement / Summary / Purged Status	Summary
Type	Special
Reviewed By Third Party	N
Expedited Review