FDA 510(k) Application Details - K231937

Device Classification Name	Dressing, Wound, Drug   More FDA Info for this Device
510(K) Number	K231937
Device Name	Dressing, Wound, Drug
Applicant	Bionova Medical, Inc. 3012 Centre Oak Way, Suite 102 Germantown, TN 38138 US Other 510(k) Applications for this Company
Contact	Alex Greene Other 510(k) Applications for this Contact
Regulation Number	000.0000   More FDA Info for this Regulation Number
Classification Product Code	FRO Other 510(k) Applications for this Device   More FDA Info for this Product Code
Date Received	06/30/2023
Decision Date	11/13/2023
Decision	SESE - SUBST EQUIV
Classification Advisory Committee	-
Review Advisory Committee	SU - General & Plastic Surgery
Statement / Summary / Purged Status	Summary
Type	Traditional
Reviewed By Third Party	N
Expedited Review