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Home » NuVasive Receives FDA 510(k) Clearance for Pediatric Implant
NuVasive Receives FDA 510(k) Clearance for Pediatric Implant
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September 8, 2017
The FDA cleared NuVasive’s redesigned Magec system with its Reline Small Stature system for pediatric use.
The Magec system uses magnets within adjustable growing rods to treat early-onset scoliosis. Reline Small Stature is a designed to provide optimal strength with a reduced implant profile.
The device is the only small stature system compatible with the 5.0 millimeter Magec rod.
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