/PRNewswire/ Empirical Spine, Inc., a medical device company creating a new class of spinal implant, recently completed the final step in the U.S. Food &.
/PRNewswire/ Empirical Spine, Inc., a medical device company creating a new class of spinal implant that works in parallel with the natural structures of.
EMPIRICAL SPINE SUBMITS PMA MODULE II FOR LIMIFLEX™ AS A NEW MOTION-PRESERVING, MINIMALLY INVASIVE STANDARD IN SPINE SURGERY streetinsider.com - get the latest breaking news, showbiz & celebrity photos, sport news & rumours, viral videos and top stories from streetinsider.com Daily Mail and Mail on Sunday newspapers.
Empirical Spine Receives FDA Breakthrough Device Designation for the LimiFlex Device Targeting Degenerative Spondylolisthesis
The Breakthrough Devices Program is a voluntary program for certain medical devices and device-led combination products that provide for more effective treatment or diagnosis of life-threatening or irreversibly debilitating diseases or conditions.
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SAN CARLOS, Calif., April 1, 2021 /PRNewswire/ Empirical Spine, Inc., a company developing advanced solutions for the surgical treatment of spinal disorders, today announced that the US Food and Drug Administration (FDA) has granted Breakthrough Device Designation (BDD) for its LimiFlex™ Paraspinous Tension Band.
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