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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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