FDA 510(k) Application Details - K231996

Device Classification Name	Wrap, Sterilization   More FDA Info for this Device
510(K) Number	K231996
Device Name	Wrap, Sterilization
Applicant	Wipak OY Wipaktie 2 Nastola FI-15560 FI Other 510(k) Applications for this Company
Contact	Hanna Marttila Other 510(k) Applications for this Contact
Regulation Number	880.6850   More FDA Info for this Regulation Number
Classification Product Code	FRG Other 510(k) Applications for this Device   More FDA Info for this Product Code
Date Received	07/05/2023
Decision Date	09/07/2023
Decision	SESE - SUBST EQUIV
Classification Advisory Committee	HO - General Hospital
Review Advisory Committee	OR - Orthopedic
Statement / Summary / Purged Status	Summary
Type	Special
Reviewed By Third Party	N
Expedited Review