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AxioMed LLC Submits Final Module III to the FDA Becoming the First and Only Lumbar Viscoelastic Total Disc Replacement Company to Complete a USA IDE Clinical Trial

Malden, MA (PRWEB) August 08, 2022 AxioMed LLC shows its determination to press forward on its FDA submission of Module III documents needed to get FDA

Spine Surgeons Using Inspan As Their Preferred Posterior Fixations For Lateral Interbody Fusion

AxioMed LLC Files PMA Module II of III targeting 2022 FDA Approval of The First and Only Viscoelastic Lumbar Disc Replacement to Complete an IDE Clinical Study

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