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The first artificial disc replacement in the U.S. was performed in 2000, but the technology has come a long way since then, with many surgeons predicting the procedure eventually will overtake spinal fusion as the standard of care.

The FDA's Breakthrough Devices Program is designed to accelerate the development, assessment and review of medical devices that provide effective treatment or diagnosis of life-threatening or irreversibly debilitating diseases or conditions.

Lakeshore Bone and Joint Institute in Chesterton, Ind., experienced a data breach involving its email system, according to data the organization shared with the Maine attorney general's office Nov. 15.

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