ArthroTAK, LLC FDA Approvals

0 new drug approvals and 2 device clearances on file. This applicant is not matched to a listed company.

Newest first

A new drug approval is an original application; a 510(k) is a device shown equivalent to one already sold.

Product	What it is	Route	Decided
ArthroTAK Tendon Anchor Kit510(k)Sep 2, 2026Orthopedic	Orthopedic	510(k)Substantially Equivalent (Special)	Sep 2, 2026
ArthroTAK Tendon Anchor Kit510(k)May 1, 2026Orthopedic	Orthopedic	510(k)Substantially Equivalent (Traditional)	May 1, 2026