FDA grants 510(k) clearance to Meditech’s new lumbar fusion device

Posted on Posted in Industry News

The US Food and Drug Administration (FDA) has granted 510(k) clearance to market spinal implants provider Meditech’s new Talos Lumbar (HA) Peek IBF lumbar fusion device. The Talos Lumbar (HA) Peek IBF is indicated for use in skeletally mature patients suffering from degenerative disc disease (DDD), which is characterised by the discogenic back pain of […]