FDA 510(k) Application Details - K221364

Device Classification Name	Fastener, Fixation, Nondegradable, Soft Tissue   More FDA Info for this Device
510(K) Number	K221364
Device Name	Fastener, Fixation, Nondegradable, Soft Tissue
Applicant	Medos International SARL Chemin-Blanc 38, Case Postale Le Locle CH 2400 CH Other 510(k) Applications for this Company
Contact	Ashley Aromando (Goncalo) Other 510(k) Applications for this Contact
Regulation Number	888.3040   More FDA Info for this Regulation Number
Classification Product Code	MBI Other 510(k) Applications for this Device   More FDA Info for this Product Code
Date Received	05/11/2022
Decision Date	07/11/2022
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