Tornier S.A.S. FDA Approvals

0 new drug approvals and 4 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
BLUEPRINT Patient Specific Instrumentation510(k)Feb 21, 2024Orthopedic	Orthopedic	510(k)Substantially Equivalent (Traditional)	Feb 21, 2024
Blueprint Mixed Reality system510(k)Jan 20, 2023Neurology	Neurology	510(k)Substantially Equivalent (Traditional)	Jan 20, 2023
Tornier Pyrocarbon Humeral Head510(k)Dec 16, 2022Orthopedic	Orthopedic	510(k)Unknown (Post-NSE)	Dec 16, 2022
BLUEPRINT Patient Specific Instrumentation510(k)Apr 15, 2021Orthopedic	Orthopedic	510(k)Substantially Equivalent (Traditional)	Apr 15, 2021