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Zdrowie i gospodarka · 06/09/2000

FDA Releases Draft Guidance for Totally Implanted Spinal Cord Stimulators

The FDA is releasing a draft guidance document for the industry on special controls for totally implanted spinal cord stimulators intended for pain relief, following a panel recommendation to reclassify these devices from class III to class II.

Source: Federal Register — Food and Drug AdministrationOpen original release →