FDA 510(k) Application Details - K220275

Device Classification Name	Appliance, Fixation, Spinal Intervertebral Body   More FDA Info for this Device
510(K) Number	K220275
Device Name	Appliance, Fixation, Spinal Intervertebral Body
Applicant	Evolution Spine 2300 N. Haskell Ave Dallas, TX 75204 US Other 510(k) Applications for this Company
Contact	Todd Wallenstein Other 510(k) Applications for this Contact
Regulation Number	888.3060   More FDA Info for this Regulation Number
Classification Product Code	KWQ Other 510(k) Applications for this Device   More FDA Info for this Product Code
Date Received	01/31/2022
Decision Date	03/18/2022
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