JillMedicalBiller
Contributor
Good afternoon!
I need some input on billing the Libre 14, Libre 2 and Libre 3 CGM systems! I've been told by Abbott that all of their Libre Freestyle systems are CLASS III devices, which my understanding is, that when billing Medicare, I use the modifier KF to designate the sensors and the readers as a Class III device.
But when I checked on the FDA web site, they say that the Abbott Freestyle systems are all Class II devices.
Is there something I'm missing in all this? Does anybody have any experience or input on billing the KF modifier for CGM readers and supplies?
Thank you for any input on this! I really appreciate it!
I need some input on billing the Libre 14, Libre 2 and Libre 3 CGM systems! I've been told by Abbott that all of their Libre Freestyle systems are CLASS III devices, which my understanding is, that when billing Medicare, I use the modifier KF to designate the sensors and the readers as a Class III device.
But when I checked on the FDA web site, they say that the Abbott Freestyle systems are all Class II devices.
Is there something I'm missing in all this? Does anybody have any experience or input on billing the KF modifier for CGM readers and supplies?
Thank you for any input on this! I really appreciate it!