I-FDA ivuma iNkqubo yokuKhiwa kwePedicle ngokuManyaniswayo

Inkqubo ye-screw ye-thoracolumbar pedicle, i-brand name OsteoCentric Spine MIS Pedicle Fastener System, eyenziwe yi-OsteoCentric Technologies, ngokuqinisekileyo, "ihloselwe ukulungiswa kunye nokuzinziswa kwamacandelo omqolo kwizigulane ezikhulileyo zamathambo njengonyango oludibeneyo lwe-acute kunye ne-thoracic, i-lumbar kunye ne-deconic instformity"
Ngokukodwa, izikrufu ze-pedicle zenzelwe "ukulungiswa kwe-pedicle engeyiyo yesibeleko kwezi zibonakaliso zilandelayo:
I-thoracolumbosacral pedicle screw system iyafana ne-Altus Partners, LLC thoracolumbosacral pedicle screw system.
Ngokutsho kwe-OsteoCentric, i-OsteoCentric Pedicle Screw Fastener System™ iya kuba neteknoloji ye-UnifiMI. Kwi-press release, u-Eric Brown, uMseki kunye ne-CEO ye-OsteoCentric, wachaza, "Inkqubo yokunamathisela i-UnifiMI stem iya kuba yinkqubo kuphela kwiimarike esebenzisa iteknoloji yokudibanisa umatshini ukuphelisa ukungazinzi kokufakelwa kwi-bone-implant interface."
Ngemvume ye-FDA 510 (k) ye-pedicle screw system, i-OsteoCentric ifumene umfutho owongezelelweyo kwimarike kunye ne-FDA 510 (k) imvume yenkqubo yayo edibeneyo ye-sacroiliac kunye nengxowa-mali yokukhula kwenkunzi ekhokelwa ngabacebisi be-OnPoint. ISiseko siya kuxhasa ukuhlanganiswa koomatshini kwi-orthopedics kunye namazinyo.