Five Steps to Medical Device Commercialization in the United States

Bringing medical devices to the market in the United States is a complex process that requires an in depth understanding of all that is involved in classifying a device, preparing a premarket submission and submitting to the FDA. To help guide manufacturers through the process of bringing medical devices to the U.S. market, this whitepaper takes you step by step through the process of submitting your medical devices for approval from the FDA.

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