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Home » Minnetronix Medical wins FDA clearance for neurosurgical access port

Minnetronix Medical wins FDA clearance for neurosurgical access port

September 9, 2020 By Chris Newmarker

The MindsEye neurosurgical access port Minnetronix Medical
The MindsEye neurosurgical access port [Image courtesy of Minnetronix Medical]
The FDA has cleared Minnetronix Medical‘s MindsEye neurosurgical access port for deep brain surgeries, the company announced today.

The clearance represents an expansion beyond the St. Paul, Minn.–based contract manufacturer’s traditional offerings.

“This extension of our business represents an additional way to partner with customers. We have the opportunity to offer them products they can integrate into their own portfolios and bring to market,” Minnetronix Medical CEO Jeremy Maniak said in a statement provided to MassDevice‘s sister site Medical Design & Outsourcing.

Read the full story on MDO.

Filed Under: 510(k), Contract Manufacturing, Featured, Neurological, Regulatory/Compliance, Surgical Tagged With: Minnetronix Medical

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About Chris Newmarker

Chris Newmarker is the executive editor of WTWH Media life science's news websites and publications including MassDevice, Medical Design & Outsourcing and more. A professional journalist of 18 years, he is a veteran of UBM (now Informa) and The Associated Press whose career has taken him from Ohio to Virginia, New Jersey and, most recently, Minnesota. He’s covered a wide variety of subjects, but his focus over the past decade has been business and technology. He holds bachelor’s degrees in journalism and political science from Ohio State University. Connect with him on LinkedIn or email at [email protected].

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