FDA 510(k) Applications Submitted by Tara Rudrapatna

FDA 510(k) Number	Submission Date	Device Name	Applicant
K243817	12/12/2024	Scorpio Universal Dome Patella; Scorpio Total Stabilizer Insert; Scorpio-Flex Posterior Stabilized Tibial Insert; Scorpio-Flex Cruciate Retaining Tibial Insert; Scorpio NRG Tibial Bearing Insert û Cruciate Retaining Insert; Scorpio NRG Tibial Bearing Inse	Howmedica Osteonics Corp. dba Stryker Orthopaedics