FDA 510(k) Application Details - K234089

Device Classification Name	Device, Anti-Snoring   More FDA Info for this Device
510(K) Number	K234089
Device Name	Device, Anti-Snoring
Applicant	Vivos Therapeutics 300 S 5th Street Murray, KY 42017 US Other 510(k) Applications for this Company
Contact	Kimberly Griffith Other 510(k) Applications for this Contact
Regulation Number	872.5570   More FDA Info for this Regulation Number
Classification Product Code	LRK Other 510(k) Applications for this Device   More FDA Info for this Product Code
Date Received	12/22/2023
Decision Date	09/16/2024
Decision	SESE - SUBST EQUIV
Classification Advisory Committee	DE - Dental
Review Advisory Committee	DE - Dental
Statement / Summary / Purged Status	Summary
Type	Traditional
Reviewed By Third Party	N
Expedited Review