Spinal Tech

Chad Campion, MD, a spine surgeon at Baptist Memorial Hospital in Memphis, Tenn., was the first surgeon to used the 7D Flash navigation system in combination with the Firebird spinal fixation system, devicemaker Orthofix said in a Feb. 25 LinkedIn post.

FloSpine's 3D-printed Ti-Largo earned FDA 510(k) clearance, the devicemaker said Feb. 28.

NuVasive's Pulse spine platform surpassed 2,000 commercial cases since it was released in 2021, CEO Chris Barry said in a fourth-quarter earnings call.

Globus Medical and NuVasive both raked in more than $1 billion in 2022 revenue, along with fourth quarter sales increases ahead of their planned merger.

Stryker, Johnson & Johnson and Zimmer Biomet posted their fourth quarter financial results, and data on their orthopedic sales.

Spinal implant company Expanding Innovations has received FDA 510(k) clearance for its X-Pac Expandable Lateral Cage System, a non-screw-based implant that addresses the core principles of lateral lumbar interbody fusion. 

NuVasive's Modulus cervical interbody implant was approved by the FDA for use with a bone void filler, the devicemaker said Feb. 21.

Medtronic on Feb. 21 posted $7.7 billion in revenue during the third quarter of fiscal year 2023.

Here are five spine devices that have recently gained FDA clearance that Becker's has reported on since Jan. 17:

Medical technology company Stryker has earned 510(k) FDA clearance for its Q Guidance System with Cranial Guidance Software.