Results showed anterior lumbar interbody fusion with posterior pedicle screw fixation may be effective and cost efficient and pose minimal complications within the immediate postoperative period when ...
Cerapedics’ PearlMatrix P-15 peptide enhanced bone graft earned expanded FDA clearance for lumbar degenerative disc disease ...
Please provide your email address to receive an email when new articles are posted on . The desire for a minimally invasive technique to restore intervertebral disc height for indirect decompression ...
Spineology Inc., the pioneer in conforming patient-specific expandable implant technology, today announced the launch of ...
BURNSVILLE, Minn., June 21, 2022 /PRNewswire/ --Inspired Spine reached the milestone of completing 1,500 Oblique Lateral Lumbar Interbody Fusion (OLLIF) procedures. This minimally invasive surgical ...
While the number of spinal fusion procedures has increased dramatically over the last 20-plus years, the biomaterials from which spinal interbody fusion devices are manufactured have not changed ...
MEQUON, Wis.--(BUSINESS WIRE)--Titan Spine, a medical device surface technology company focused on developing innovative surface-enhanced spinal interbody fusion implants, reports that the U.S.
Cerapedics Inc., a global, commercial-stage orthopedics company dedicated to redefining the path to bone repair, today announced U.S. Food and Drug Administration (FDA) approval for an expansion to ...
Posterior lumbar interbody fusion (PLIF) and transforaminal lumbar interbody fusion (TLIF) procedures are coded 22630 for a lumbar initial interspace arthrodesis, posterior interbody technique, which ...
Here are 40 spine devices and technologies earning FDA clearances in 2025. Note: This is not an exhaustive list. 1. SurGenTec earned FDA 510(k) clearance for its OsteoFlo HydroFiber to be used as a ...
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