FDA 510(k) Application Details - K193373

Device Classification Name	More FDA Info for this Device
510(K) Number	K193373
Device Name	Comprehensive« Reverse Shoulder
Applicant	Biomet Inc. 56 East Bell Drive, PO Box 587 Warsaw, IN 46581 US Other 510(k) Applications for this Company
Contact	Kari Hovorka 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	12/05/2019
Decision Date	04/15/2020
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