Philips Receives FDA Approval For Enhanced 160cm LumiGuide Guidewire, Marking 1000th Procedure Using Fiber Optic RealShape (FORS) Technology; First Use By Vascular Surgeon Carlos Timaran For Complex Aortic Repair
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Philips has received FDA approval for its enhanced 160cm LumiGuide Guidewire, marking a milestone with the 1000th procedure using its Fiber Optic RealShape (FORS) technology. The first use of this guidewire was by vascular surgeon Carlos Timaran for a complex aortic repair.
September 17, 2024 | 1:00 pm
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Philips has received FDA approval for its enhanced LumiGuide Guidewire, marking a significant milestone with the 1000th procedure using FORS technology. This approval and milestone could enhance Philips' reputation and market position in medical technology.
The FDA approval of Philips' enhanced LumiGuide Guidewire is a significant regulatory achievement, likely to boost investor confidence and enhance Philips' market position in the medical technology sector. The milestone of the 1000th procedure using FORS technology further solidifies its reputation for innovation.
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RELEVANCE 90