FDA 510(k) Applications Submitted by Lisa Stahl

FDA 510(k) Number Submission Date Device Name Applicant
K211359 05/03/2021 Tornier PerformÖ Patient-Matched Primary Reversed Glenoid and BLUEPRINTÖ Patient Specific Instrumentation Tornier, Inc.
K213124 09/27/2021 Tomier PerformÖ Reversed Glenoid Cannulated Glenospheres Tornier, Inc.


Search | Companies | Product Codes | Device Names | Contacts | Applications | Decisions | Contact