DeviceClearance

OptiMesh Multiplanar Expandable Interbody Fusion System— 510(k) K231781

Substantially Equivalent

Spineology, Inc.

FDA 510(k) clearance K231781 for OptiMesh Multiplanar Expandable Interbody Fusion System, Substantially Equivalent on 2023-10-18. Applicant: Spineology, Inc..

Clearance details

Applicant
Spineology, Inc.
Product code
Code OQB
Advisory panel
Orthopedic
Date received
Decision date
Decision
Substantially Equivalent
Clearance type
Special
Location
Saint Paul, MN, US
Download summary PDFView on FDA.gov ↗

Data sourced from openFDA. This site is unofficial and independent of the FDA.