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Amplify Surgical, Inc.

FDA 510(k) & PMA Approved Devices — 3 products

Total Devices3
Categories1
Latest Approval2022-10-18
TypeNumberDevice NameCodeDate
510(k) K222203 DualXSLIM(R) T/PLIF MAX 2022-10-18 View
510(k) K211740 DualX MAX 2021-09-29 View
510(k) K192434 DualX Lumbar Intervertebral Body Fusion Device MAX 2019-10-15 View
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