Processed nerve allografts and synthetic nerve conduits for peripheral nerve gap repair
Defines medical necessity and investigational indications for use of processed nerve allografts and synthetic nerve conduits to repair peripheral nerve gaps in Commercial and Medicare members, including contraindications and prior authorization requirements. Specifies gap-length–based criteria and limitations (e.g., maximum allograft length 70 mm) and scenarios where conduits are medically necessary.
New medical policy describing medically necessary and investigational indications.