Medical Device Manufacturer · US , Clearwater , FL

Interbody Innovations, Llp

4 submissions · 1 cleared · Since 2005
4
Total
1
Cleared
0
Denied

Interbody Innovations, Llp has 1 FDA 510(k) cleared medical devices. Based in Clearwater, US.

Historical record: 1 cleared submissions from 2005 to 2008. Primary specialty: Orthopedic.

Browse the FDA 510(k) cleared devices submitted by Interbody Innovations, Llp Filter by specialty or product code using the sidebar.

4 devices
1–4 of 4
ZEUS SMALL CERVICAL CAGE AND LARGE, EXTRA LARGE, CURVED AND STRAIGHT LUMBAR CAGES
K081614 · ODP Intervertebral Fusion Device With Bone Graft, Cervical · Orthopedic
Sep 2008 88d
PEEK SPINAL SPHERES
K073105 · NVR Intervertebral Fusion Device With Bone Graft, Solid-sphere, Lumbar · Orthopedic
Jan 2008 62d
SPINAL SPHERES
K062992 · NVR Intervertebral Fusion Device With Bone Graft, Solid-sphere, Lumbar · Orthopedic
Jul 2007 298d
INTERBODY INNOVATIONS CEMENT RESTRICTOR
K051371 · JDK Prosthesis, Hip, Cement Restrictor · Orthopedic
Dec 2005 194d
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