FDA 510(k) Applications Submitted by Jesse Albright

FDA 510(k) Number Submission Date Device Name Applicant
K240566 02/29/2024 Reef L Interbody System; WaveForm L Interbody System SeaSpine Orthopedics Corporation
K240830 03/26/2024 Reef TO/TA System; Regatta Lateral System; Explorer TO System; WaveForm C Interbody System; WaveForm TO Interbody System; WaveForm TA Interbody System; FORZA XP Expandable Spacer System; Shoreline ACS Interbody System; Shoreline RT Interbody System; Merid Orthofix Medical Inc.
K250987 03/31/2025 aprevo« posterior/transforaminal lumbar interbody fusion device Carlsmed Inc.
K241466 05/23/2024 Shoreline ACS Interbody System; Shoreline RT Interbody System; Regatta Lateral System; Reef L Interbody System; Reef TO/TA System; Meridian Interbody System; WaveForm C Interbody System; WaveForm L Interbody System; WaveForm TO Interbody System; WaveForm SeaSpine Orthopedics Corporation
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
K233694 11/17/2023 Meridian Interbody System; 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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