FDA 510(k) Applications Submitted by Brianna Prindle

FDA 510(k) Number Submission Date Device Name Applicant
K241482 05/24/2024 Kinos Total Ankle System restor3d
K242356 08/08/2024 TIDAL Fusion Cage System restor3d, Inc.
K232595 08/25/2023 Kinos Axiom Total Ankle System restor3d
K242868 09/20/2024 Kinos Total Ankle System restor3d
K223326 10/31/2022 Axiom PSR System Restor3d
K243643 11/26/2024 restor3d Reverse Total Shoulder Arthroplasty System restor3d
K243768 12/06/2024 iTotal« IdentityÖ Cruciate Retaining 3DP Porous Knee Replacement System restor3d, inc.


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