FDA 510(k) Application Details - K191764

Device Classification Name	Filler, Bone Void, Calcium Compound   More FDA Info for this Device
510(K) Number	K191764
Device Name	Filler, Bone Void, Calcium Compound
Applicant	Inion Oy LΣΣkΣrinkatu 2 Tampere 33520 FI Other 510(k) Applications for this Company
Contact	Tiina Tyni Other 510(k) Applications for this Contact
Regulation Number	888.3045   More FDA Info for this Regulation Number
Classification Product Code	MQV Other 510(k) Applications for this Device   More FDA Info for this Product Code
Date Received	07/01/2019
Decision Date	07/31/2019
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