Empirical Spine
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Regulatory
Empirical Spine Completes Full Premarket Approval (PMA) Submission to FDA for LimiFlex™ Dynamic Sagittal Tether™
LimiFlex™ DST™ Is Designed for a New Class of Lumbar Stabilization Surgery That Meets the Demands of Value-Based Care. SAN…
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Spine
Empirical Spine Advances LimiFlex™ As A New Motion-Preserving, Minimally Invasive Standard In Spine Surgery
SAN CARLOS, Calif., Feb. 1, 2022 /PRNewswire/ — Empirical Spine, Inc., a medical device company creating a new class of spinal implant…
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Regulatory
Empirical Spine Receives FDA Breakthrough Device Designation for the LimiFlex Device Targeting Degenerative Spondylolisthesis
SAN CARLOS – 31 March 2021 – Empirical Spine, Inc., a company developing advanced solutions for the surgical treatment of spinal…
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Empirical Spine Initiates PMA Submission Process for FDA Approval of LimiFlex for Degenerative Spondylolisthesis
San Carlos, Calif. – February 23, 2021 – Empirical Spine, Inc., maker of the LimiFlex™ Paraspinous Tension Band, today announced…
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