SpineGuard passes inspection for product registration in Brazil

SpineGuard passed inspection for certification from the Brazilian government regulatory authority after a three-day inspection in Paris, where the company has headquarters.

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SpineGuard, maker of the PediGuard device for safe screw placement during spine surgery, received the certification shortly after the ANVISA made it mandatory for registering to market a new device in Brazil.

 

“This ANVISA certification consolidates our regulatory position in Brazil, an important market for SpineGuard,” said Co-Founder and CEO Pierre Jerome. “It will allow us to initiate the registration process for the Curved, Cannulated and XS versions of PediGuard in this large market.”

 

More articles on orthopedic devices:
10 core concepts for the surgical navigation systems market
Centinel Spine releases next generation anterior lumbar spine device—5 things to know
10 key thoughts on the spinal non-fusion device market

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