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FDA 510(k) Applications Submitted by Cindy Toyama
FDA 510(k) Number
Submission Date
Device Name
Applicant
K230486
02/23/2023
Cove Strip
SeaSpine Orthopedics Corporation
K231030
04/11/2023
Cove Putty, OsteoCove Putty
SeaSpine Orthopedics Corporation
K232668
09/01/2023
Cove Strip, OsteoCove Strip
SeaSpine Orthopedics Corporation
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