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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.
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