FDA 510(k) Application Details - K190375

Device Classification Name	Fastener, Fixation, Nondegradable, Soft Tissue   More FDA Info for this Device
510(K) Number	K190375
Device Name	Fastener, Fixation, Nondegradable, Soft Tissue
Applicant	Parcus Medical, LLC 6423 Parkland Dr Sarasota, FL 34243 US Other 510(k) Applications for this Company
Contact	Paul Vagts 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	02/19/2019
Decision Date	04/24/2019
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