FDA 510(k) Application Details - K242253

Device Classification Name	More FDA Info for this Device
510(K) Number	K242253
Device Name	JARVIS Glenoid Reverse Shoulder Prosthesis
Applicant	FH Industrie 6 Rue Nobel, Zi De Kernevez Quimper 29000 FR Other 510(k) Applications for this Company
Contact	Naoual Rahimi Other 510(k) Applications for this Contact
Regulation Number	More FDA Info for this Regulation Number
Classification Product Code	PHX Other 510(k) Applications for this Device   More FDA Info for this Product Code
Date Received	07/31/2024
Decision Date	11/25/2024
Decision	SESE - SUBST EQUIV
Classification Advisory Committee	OR - Orthopedic
Review Advisory Committee	OR - Orthopedic
Statement / Summary / Purged Status	Summary
Type	Traditional
Reviewed By Third Party	N
Expedited Review