FDA 510(k) Application Details - K191746

Device Classification Name	More FDA Info for this Device
510(K) Number	K191746
Device Name	SMR TT Augmented Glenoid System
Applicant	Limacorporate S.p.A via Nazionale 52 Villanova di San Daniele del Friuli 33038 IT Other 510(k) Applications for this Company
Contact	Michela Zanotto 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	07/01/2019
Decision Date	11/22/2019
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