6 个月
GlobalData on MSNAmphix Bio obtains FDA breakthrough device status for bone regeneration productAmphix Bio has received a breakthrough device designation from the US Food ... disease through transforaminal lumbar ...
To follow up on the completion of its clinical proof-of-concept study, SynerFuse™ and its partner, Velentium Medical, today announced plans to scale the patented SynerFuse™ e-TLIF™ procedure implant ...
"Requiring only a single incision and involving direct visual placement of the neurostimulation device will make the SynerFuse™ e-TLIF™ procedure better in terms of patient safety," said ...
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