FDA Product Code OVD: Intervertebral Fusion Device With Integrated Fixation, Lumbar
Under FDA product code OVD, lumbar intervertebral fusion devices with integrated fixation are cleared for combined interbody fusion and segmental stabilization.
These devices integrate both the interbody spacer and fixation elements — typically screws or blades — into a single implant, eliminating the need for separate posterior instrumentation in some patients. They are used in minimally invasive lumbar fusion procedures.
OVD devices are Class II medical devices, regulated under 21 CFR 888.3080 and reviewed by the FDA Orthopedic panel.
Leading manufacturers include Nu Vasive, Incorporated, Medacta International S.A. and Nexus Spine, LLC.
199
Total
199
Cleared
130d
Avg days
2007
Since
199 devices
Cleared
Feb 12, 2018
CASCADIA Interbody System
K2m
Orthopedic
139d
Cleared
Nov 02, 2017
SOVEREIGN™ Spinal System
Medtronic Sofamor Danek USA, Inc.
Orthopedic
92d
Cleared
Sep 25, 2017
INDEPENDENCE® Spacers
Globus Medical, Inc.
Orthopedic
250d
Cleared
Apr 26, 2017
NuVasive BASE Interfixated Titanium System
Nu Vasive, Incorporated
Orthopedic
57d
Cleared
Mar 16, 2017
MectaLIF Anterior Stand Alone
Medacta International S.A.
Orthopedic
29d