A predicate device is an existing previously cleared 510k Certification and is marketed under a regulatory pathway that is used for the comparison between the proposed device to prove the substantial equivalent.Multiple predicates can also be used for comparing the substantial equivalence when the proposed device has more than one intended use, but it is better to compare the substantial equivalent with one single predicate device.
Predicate devices are selected based on
Predicate device identifications are verified when stating substantial equivalence and if the FDA 510k submission is provided with an incorrect predicate device, then FDA holds or withdraws the submission.substantial equivalentIt means when the proposed device is the same as the predicate device and is safe and efficient for the user. Which has the same device intended use and similar technological characteristics.Technological characteristics – performance testing, clinical testing, an additional requirement.
The device is said to be substantially equivalent if it has:
Or
Decision making of substantial equivalence for a 510K
Or
Difference between substantial equivalence and predicate device
PREDICATE DEVICE | SUBSTANTIAL EQUIVALENCE |
It is a legally marketed device | It is a method to find the SE of the proposed device |
It is used to find if the newly proposed device is safe and effective by comparing with the predicate device. | Comparison method between predicate device and proposed device to find the substantial equivalence. |