FDA 510(k) Applications Submitted by Jesse Albright

FDA 510(k) Number Submission Date Device Name Applicant
K211606 05/25/2021 Mariner Deformity System SeaSpine Orthopedics Corporation
K231654 06/06/2023 NorthStar OCT System SeaSpine Inc.
K222110 07/18/2022 Mariner RDX System SeaSpine Orthopedics Corporation
K212692 08/25/2021 Mariner Pedicle Screw System SeaSpine Orthopedics Corporation
K222732 09/09/2022 WaveForm A Interbody System SeaSpine Orthopedics Corporation
K193224 11/22/2019 Daytona« Small Stature Growth Rod Conversion Set SeaSpine Orthopedics Corporation


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