K062992 is the FDA 510(k) clearance record for SPINAL SPHERES, a class III device, cleared for Interbody Innovations, Llp on under FDA product code NVR (Intervertebral Fusion Device With Bone Graft, Solid-Sphere, Lumbar). FDA's definition for product code NVR reads: "Intended to be inserted between the vertebral bodies into the disc space from l3 to s1 to provide stabilization and to help promote intervertebral body fusion. To be used with bone graft, for holding bone parts in alignment while they...". FDA records list 4 510(k) clearances for Interbody Innovations, Llp, from to . As of , FDA records show no recalls naming K062992.
Clearance record
Decision date
Received
(298 days to decision)
Product code
NVR Intervertebral Fusion Device With Bone Graft, Solid-Sphere, Lumbar
