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 Globus Medical, Inc., Nu Vasive, Incorporated and K2m, Inc..
203
Total
203
Cleared
129d
Avg days
2007
Since
203 devices
Cleared
Aug 28, 2008
BLACKSTONE PILLAR SA PARTIAL VERTEBRAL BODY REPLACEMENT DEVICE
Blackstone Medical, Inc.
Orthopedic
59d
Cleared
Jul 02, 2008
VU APOD INTERVERTABRAL BODY FUSION DEVICE
Theken Spine, LLC
Orthopedic
100d
Cleared
Jul 02, 2008
SOLITAIRE ANTERIOR SPINAL SYSTEM
Biomet Spine
Orthopedic
34d
Cleared
Jun 25, 2008
SOLITAIRE PEEK-OPTIMA ANTERIOR SPINAL SYSTEM
Biomet Spine
Orthopedic
37d
Cleared
Oct 12, 2007
SYNFIX-LR SPACER
Synthes Spine Co.Lp
Orthopedic
59d