Here are six things to know:
1. Dr. Scully implanted the system during an outpatient procedure on Oct. 20.
2. The FDA cleared Huntley, Ill.-based Life Spine’s PRO-LINK Ti in September.
3. The system is a low-profile, standalone cervical interbody device.
4. The device features the company’s Osseo-Loc technology, which is a surface treatment for titanium with 500 microns to 600 microns of porosity.
5. Life Spine anticipates a full product release of the PRO-LINK Ti system by the end of 2016.
6. Dr. Scully completed his neurological surgery residency at the Indiana University School of Medicine in Indianapolis.
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OrthoCarolina completes 100th Mazor Robotics surgical case: 3 things to know
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