FDA 510(k) Application Details - K230142

Device Classification Name	Splint, Intranasal Septal   More FDA Info for this Device
510(K) Number	K230142
Device Name	Splint, Intranasal Septal
Applicant	BioMed ENT, Inc. 18911 Hardy Oak Blvd San Antonio, TX 78258 US Other 510(k) Applications for this Company
Contact	Antonius Voermans Other 510(k) Applications for this Contact
Regulation Number	874.4780   More FDA Info for this Regulation Number
Classification Product Code	LYA Other 510(k) Applications for this Device   More FDA Info for this Product Code
Date Received	01/18/2023
Decision Date	03/22/2023
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