FDA 510(k) Applications Submitted by SPINEART SA

FDA 510(k) Number Submission Date Device Name Applicant
K240699 03/14/2024 SCARLET« AC-Ti Spineart SA
K241321 05/10/2024 Juliet« Ti LL Lumbar Interbody Device Spineart SA
K241644 06/07/2024 SPINEART Navigation Instrument System Spineart SA
K242589 08/30/2024 Scarlet« AL-T Spineart SA
K242890 09/23/2024 SPINEART Navigation Instrument System SPINEART SA
K242933 09/25/2024 SPINEART Navigation Instrument System Spineart SA
K230583 03/02/2023 Tryptik Ti Spineart SA
K231069 04/14/2023 PERLA« TL Posterior Thoraco-lumbar Fixation System Spineart SA
K183630 12/26/2018 SPINEART Navigation Instrument System Spineart SA


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