FDA 510(k) Application Details - K232583

Device Classification Name	More FDA Info for this Device
510(K) Number	K232583
Device Name	Catalyst R1 Reverse Shoulder System
Applicant	Catalyst OrthoScience, Inc. 14710 Tamiami Trail N. Naples, FL 34110 US Other 510(k) Applications for this Company
Contact	Dale Davison 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	08/25/2023
Decision Date	09/20/2023
Decision	SESE - SUBST EQUIV
Classification Advisory Committee	OR - Orthopedic
Review Advisory Committee	OR - Orthopedic
Statement / Summary / Purged Status	Summary
Type	Special
Reviewed By Third Party	N
Expedited Review