Medicrea has filed a 510(k) submission with FDA for 3D-printed titanium interbody devices, with compatible UNiD™ Lab surgical planning and analytical services. Clearance is expected by year-end.
UNiD™ Rods, a patient-specific spinal implant, received FDA 510(k) clearance in late 2014. The system passed the 1,000-procedure milestone in late 2016.
Medicrea has filed a 510(k) submission with FDA for 3D-printed titanium interbody devices, with compatible UNiD™ Lab surgical planning and analytical services. Clearance is expected by year-end.
UNiD™ Rods, a patient-specific spinal implant, received FDA 510(k) clearance in late 2014. The system passed the 1,000-procedure milestone in late...
Medicrea has filed a 510(k) submission with FDA for 3D-printed titanium interbody devices, with compatible UNiD™ Lab surgical planning and analytical services. Clearance is expected by year-end.
UNiD™ Rods, a patient-specific spinal implant, received FDA 510(k) clearance in late 2014. The system passed the 1,000-procedure milestone in late 2016.
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