FDA panel meeting on orthopedic devices rescheduled for May

04/11/2013 | MassDevice.com (Boston)

An FDA panel meeting to consider whether to continue to subject shortwave diathermy systems to the premarket approval process or recategorize them as Class I or II devices has been rescheduled for May 21. The panel will also meet May 22 to discuss the possible reclassification of pedicle screws, which are used in spinal fusion surgeries.

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MassDevice.com (Boston)

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