I-FDA Ivuma Inkqubo Yesikrufu SeePedicle Ezihlanganisiweyo Ngoomatshini

Inkqubo yezikrufu ze-thoracolumbar pedicle, egama lingu-OsteoCentric Spine MIS Pedicle Fastener System, eyenziwe yi-OsteoCentric Technologies, ewe, “yenzelwe ukuqinisa nokuqinisa amacandelo omqolo kwizigulana ezikhulileyo zamathambo njengonyango oludibeneyo lokungazinzi okanye ukukhubazeka kwe-sacral okukhawulezileyo nokwesifuba, kwe-lumbar nakwi-chronic sacral”.
Ngokukodwa, izikrufu zepedicle zenzelwe "ukulungiswa kwepedicle engeyoyomlomo wesibeleko kwezi mpawu zilandelayo:
Inkqubo yezikrufu ze-thoracolumbosacral pedicle ngokusisiseko ifana kakhulu nenkqubo yezikrufu ze-thoracolumbosacral pedicle ze-Altus Partners, LLC.
Ngokutsho kwe-OsteoCentric, i-OsteoCentric Pedicle Screw Fastener System™ iza kubonisa iteknoloji ye-UnifiMI. Kwingxelo yabezindaba, u-Eric Brown, uMsunguli kunye ne-CEO ye-OsteoCentric, ucacisile, “Inkqubo yokuncamathisela isiqu se-UnifiMI iza kuba yinkqubo kuphela kwimarike esebenzisa iteknoloji yokudibanisa oomatshini ukuphelisa ukungazinzi kokufakelwa kwi-interface yethambo kunye ne-implant.”
Ngokuvunywa kwe-FDA 510(k) kwenkqubo yezikrufu zepedicle, i-OsteoCentric ifumene amandla angakumbi kwimarike ngokuvunywa kwe-FDA 510(k) kwenkqubo yayo yokudibanisa i-sacroiliac kunye nengxowa-mali yokukhulisa imali ekhokelwa yi-OnPoint Advisors. I-Foundation iza kuxhasa ukuhlanganiswa koomatshini kwi-orthopedics nakwi-dentistry.