FDA 510(k) Applications Submitted by Acuity Surgical Devices, LLC

FDA 510(k) Number Submission Date Device Name Applicant
K221535 05/27/2022 Align Lumbar Interbody Fusion System Acuity Surgical Devices, LLC
K201671 06/19/2020 A-Link Z Acuity Surgical Devices, LLC
K222561 08/24/2022 Align Acuity Surgical Devices, LLC


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