FDA 510(k) Applications for Medical Device Product Code: OQB ()

FDA 510(k) Applications for Medical Device Product Code "OQB"

FDA 510(k) Number	Applicant	Device Name	Decision Date
K230927	Spineology Inc.	OptiMesh Multiplanar Expandable Interbody Fusion System	11/01/2023
K231781	Spineology Inc.	OptiMesh Multiplanar Expandable Interbody Fusion System	10/18/2023
DEN200010	Spineology, Inc.	Spineology Interbody Fusion System	09/18/2020