Meditech Spine’s Talos devices receive FDA clearance for use with allograft bone graft: 3 notes

Meditech Spine’s Talos interbody devices have received FDA clearance for use with allograft comprised of cancellous or corticocancellous bone graft.

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Here are three notes:

 

1. Meditech’s interbody cervical and lumbar devices are indicated for use with autograft or allograft.

 

2. These devices include the Talos-P, Talos-T, Talos-A, Talos-L and both the Talos-C and Talos-C (HA) interbody implants.

 

3. Meditech Spine is a spinal implant company. It obtained its first FDA clearance in 2009.

 

More articles on devices:
Minimally invasive surgical instrument market forecast: 3 takeaways
joimax launches EndoLIF On-Cage, iLESSYS Delta interlaminar systems
Life Spine releases devices for expandable lateral interbody fusions

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