www.fdanews.com/articles/124187-mesynthes-obtains-fda-510-k-for-endoform-dermal-template
Mesynthes Obtains FDA 510(k) for Endoform Dermal Template
February 2, 2010
Mesynthes, a privately held regenerative medicine company, Tuesday announced
that the U.S. Food and Drug Administration (FDA) has granted 510(k) clearance for the company’s Endoform Dermal Template.
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