FDA 510(k) Application Details - K203029

Device Classification Name	Screw, Fixation, Bone   More FDA Info for this Device
510(K) Number	K203029
Device Name	Screw, Fixation, Bone
Applicant	Auxein Medical Private Limited Plot No. 168, 169, 170 Phase-IV, Sector 57, Kundli Industrial area Sonipat 131028 IN Other 510(k) Applications for this Company
Contact	Rahul Luthra 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	10/02/2020
Decision Date	08/20/2021
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