FDA 510(k) Applications Submitted by Brooks McAdam

FDA 510(k) Number Submission Date Device Name Applicant
K230942 04/03/2023 SPIRA« Posterior Lumbar Spacers Camber Spine Technologies
K232256 07/28/2023 Alcantara Thoracolumbar Plate System Camber Spine Technologies, LLC
K233972 12/15/2023 Camber Sacroiliac (SI) Fixation System Camber Spine Technologies
K223837 12/22/2022 SPIRA«-C Integrated Fixation System Camber Spine Technologies
K234077 12/22/2023 SPIRA« Anterior Lumbar Spacers Camber Spine Technologies


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