June 25, 2023
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PathKeeper Surgical receives FDA 510(k) clearance of 3D optical navigation system
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Key takeaways:
- PathKeeper Surgical received FDA 510(k) clearance of its 3D optical navigation system
- The navigation system is designed for patients undergoing spinal surgery.
PathKeeper Surgical has announced FDA 510(k) clearance of its PathKeeper 3D optical navigation system for patients undergoing spine surgery, according to a company release.
The navigation system eliminates exposure to radiation for patients in the OR, according to the release.
“We are excited to reach this important milestone for PathKeeper and the company,” Erez Lampert, founder and CEO of PathKeeper Surgical, said in the release. “We now move our focus to commercialization in the United States to make PathKeeper available to all spine surgeons and their patients,” Lampert said.
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