Astura Medical gains clearance for lateral lumbar interbody fusion device

The FDA on April 14 provided Astura Medical 510(k) clearance for its Sirion lateral lumbar interbody fusion system.

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Three insights:

1. Sirion offers a two or three blade configuration, with each blade featuring distraction and toeing capabilities.

2. An optional anterior blade allows surgeons to customize the access and rigidity of the device to fit patients’ specific anatomies.

3. Sirion features spacers in HA PEEK or Acid-etched Ti in a variety of sizes.

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