FDA 510(k) Application Details - K230841

Device Classification Name	Prosthesis, Nail   More FDA Info for this Device
510(K) Number	K230841
Device Name	Prosthesis, Nail
Applicant	JPS Corporation Toho Edogawabashi Bldg. 3F, 1-24-8 Sekiguchi, Bunkyo-ku Tokyo 112-0014 JP Other 510(k) Applications for this Company
Contact	Yasuko Kida Other 510(k) Applications for this Contact
Regulation Number	000.0000   More FDA Info for this Regulation Number
Classification Product Code	MQZ Other 510(k) Applications for this Device   More FDA Info for this Product Code
Date Received	03/28/2023
Decision Date	01/22/2024
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