United States: FDA's New Draft Guidance On 510(k) Implant Devices: What You Need To Know - Hyman, Phelps, & McNamara, P.C.

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26 Oct 2023 0 shares 1 views

United States: FDA's New Draft Guidance On 510(k) Implant Devices: What You Need To Know - Hyman, Phelps, & McNamara, P.C.

Mondaq

Published 26 Oct 2023

As we recently blogged, FDA released three draft guidance documents to help enhance the predictability, consistency, and transparency of the 510(k) program.

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United States: FDA Brings Its Formal Meetings Guidance Up To Date: What You Need To Know About Type D, INTERACT, And "In-Person" Meetings Under PDUFA - Hyman, Phelps, & McNamara, P.C.

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United States: FDA's New Draft Guidance On 510(k) Implant Devices: What You Need To Know - Hyman, Phelps, & McNamara, P.C.

United States: FDA's New Draft Guidance On 510(k) Implant Devices: What You Need To Know - Hyman, Phelps, & McNamara, P.C.

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