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Salutaris receives 510(k) clearance for radionuclide brachytherapy device

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The FDA has granted 510(k) clearance for the SMD-Sr90-DA Radionuclide Brachytherapy Source, according to a press release from Salutaris Medical Devices.

The device, indicated for episcleral brachytherapy, is to be used within a manual brachytherapy applicator system.

Salutaris’ technology is aimed at improving outcomes for wet age-related macular degeneration.