FDA 510(k) Application Details - K250215

Device Classification Name	Hearing Aid, Bone Conduction   More FDA Info for this Device
510(K) Number	K250215
Device Name	Hearing Aid, Bone Conduction
Applicant	Cochlear 10350 Park Meadows Drive Lone Tree, CO 80214 US Other 510(k) Applications for this Company
Contact	Denis DiMartino Other 510(k) Applications for this Contact
Regulation Number	874.3300   More FDA Info for this Regulation Number
Classification Product Code	LXB Other 510(k) Applications for this Device   More FDA Info for this Product Code
Date Received	01/24/2025
Decision Date	05/29/2025
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