FDA 510(k) Application Details - K233594

Device Classification Name	More FDA Info for this Device
510(K) Number	K233594
Device Name	Genesys Spine 3DP AIS-C II Cervical Interbody System
Applicant	Genesys Spine 1250 S. Capital of Texas Highway Building 3, Suite 600 Austin, TX 78746 US Other 510(k) Applications for this Company
Contact	Andrew Davison Other 510(k) Applications for this Contact
Regulation Number	More FDA Info for this Regulation Number
Classification Product Code	OVE Other 510(k) Applications for this Device   More FDA Info for this Product Code
Date Received	11/08/2023
Decision Date	12/13/2023
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