Stryker Corporation (Tornier, S.A.S.) FDA Approvals

0 new drug approvals and 2 device clearances on file. Matched by name to SYK.

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
Blueprint Patient-Specific Instrumentation510(k)Apr 3, 2026Orthopedic	Orthopedic	510(k)Substantially Equivalent (Traditional)	Apr 3, 2026
Blueprint Patient-Specific Instrumentation; Shoulder iD Primary Reversed Glenoid510(k)Oct 10, 2024Orthopedic	Orthopedic	510(k)Substantially Equivalent (Traditional)	Oct 10, 2024