Filler, recombinant human bone morphogenetic protein, collagen scaffold with metal prosthesis, osteoinduction

Filler, recombinant human bone morphogenetic protein, collagen scaffold with metal prosthesis, osteoinduction is a medical device manufactured by Medtronic Sofamor Danek USA, Inc.. It received FDA Premarket Approval (PMA) on 2016-09-29 under PMA number P000058. The device is classified under FDA product code NEK. It was reviewed by the OR advisory panel. This device is classified as Class III by the FDA. Class III devices subject to the most stringent regulatory controls. These devices generally require premarket approval (PMA) because they support or sustain human life, are of substantial importance in preventing impairment of human health, or present a potential unreasonable risk of illness or injury. PMA is the most stringent type of device marketing application required by the FDA. The device falls under the medical specialty of U. Unlike 510(k) clearance, which demonstrates substantial equivalence to a predicate device, PMA requires the manufacturer to submit clinical trial data demonstrating the safety and effectiveness of the device. PMA is generally required for Class III devices that support or sustain human life, are of substantial importance in preventing impairment of human health, or present a potential unreasonable risk of illness or injury.