FDA 510(k) Application Details - K230507

Device Classification Name	Screw, Fixation, Bone   More FDA Info for this Device
510(K) Number	K230507
Device Name	Screw, Fixation, Bone
Applicant	Zimed Medikal Mh. 03070 Cd. No:4 Gaziantep 27580 TR Other 510(k) Applications for this Company
Contact	H.Nurcan Bilgi Other 510(k) Applications for this Contact
Regulation Number	888.3040   More FDA Info for this Regulation Number
Classification Product Code	HWC Other 510(k) Applications for this Device   More FDA Info for this Product Code
Date Received	02/24/2023
Decision Date	01/04/2024
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