Does L7368 require prior authorization?

No, L7368 does not require prior authorization (high confidence). Code is covered without prior authorization.

`L7368`, Lithium ion battery charger, replacement only

HCPCS/CPT

No Prior Auth Required

Code is covered without prior authorization (high confidence)

Medical records must document the beneficiary’s current functional and physical capabilities and the expected functional potential, and must explain differences between current and expected functional states if present.
A clinical evaluation to determine the beneficiary’s functional level must be performed and documented in the medical record.
For fluid/pneumatic/electronic knee coverage for functional level 2, the medical record must document the rationale that the selected knee will improve functional outcomes (e.g., fall reduction), help accomplish ADLs, and that lower-level knee systems were considered and ruled out.
For electronic/microprocessor knee coverage at functional level 2, documentation must show the device is indicated for K2, includes stumble-recovery technology, the beneficiary can perform daily charging, and the beneficiary can understand/respond to error alerts.
For addition L5859, documentation must show an existing microprocessor knee (L5856), K3 functional level, documented spine and/or sound-limb comorbidity impairing hip extension/quadriceps that limits K3 function with microprocessor knee alone, and beneficiary ability to daily charge and respond to alerts.
Clinical justification for advanced foot/knee technologic or design features must be retained in the treating practitioner's or prosthetist's files.

A lower limb prosthesis is covered when the beneficiary is motivated to ambulate.
A lower limb prosthesis is covered when the beneficiary is expected to reach or maintain a defined functional state within a reasonable period of time.
Coverage and component selection are based on a documented functional level (K-level 0–4) determined by the treating practitioner and prosthetist considering past prosthetic use, residual limb status, comorbidities, and the beneficiary’s desire to ambulate.
Foot components L5970 or L5974 are covered for beneficiaries with functional level >=1.
Flexible-keel foot L5972 or multiaxial ankle/foot L5978 are covered for beneficiaries with functional level >=2.
Microprocessor-controlled ankle/foot (L5973), energy storing (L5976), dynamic response multi-axial (L5979), flex foot systems (L5980,L5981), or shank-foot with vertical loading pylon (L5987) are covered when the beneficiary is functional level >=3, or when functional level =2 and the beneficiary meets the level-2 knee coverage criteria and a higher-level foot is required for safe use of the prescribed knee.

L33787, Lower Limb Prostheses

UHC-POL-lower-extremity-prosthetics, Lower Extremity Prosthetics

UHC-POL-upper-extremity-prosthetic-devices, Upper Extremity Prosthetic Devices

AETNA-CPB-0578, Lower Limb Prostheses

AETNA-CPB-0399, Upper Limb Prostheses

DME104.001, Myoelectric Prosthetic and Orthotic Components for the Upper Limb

BCBSIL-DME104.012, Lower-Limb Prosthetics, Including Microprocessor-Controlled Prosthetics

BCBSIL-DME104.001, Myoelectric Prosthetic and Orthotic Components for the Upper Limb

BCBSMT-DME104.012, Lower-Limb Prosthetics, Including Microprocessor-Controlled Prosthetics

BCBSMT-DME104.001, Myoelectric Prosthetic and Orthotic Components for the Upper Limb

BCBSNM-DME104.012, Lower-Limb Prosthetics, Including Microprocessor-Controlled Prosthetics

BCBSNM-DME104.001, Myoelectric Prosthetic and Orthotic Components for the Upper Limb

BCBSOK-DME104.012, Lower-Limb Prosthetics, Including Microprocessor-Controlled Prosthetics

BCBSOK-DME104.001, Myoelectric Prosthetic and Orthotic Components for the Upper Limb

UMR-POL-UMR-lower-extremity-prosthetics, Lower Extremity Prosthetics

UMR-POL-UMR-upper-extremity-prosthetic-devices, Upper Extremity Prosthetic Devices

SUREST-POL-SUREST-lower-extremity-prosthetics, Lower Extremity Prosthetics

SUREST-POL-SUREST-upper-extremity-prosthetic-devices, Upper Extremity Prosthetic Devices

Ask Verity about documentation requirements, denial risks, or coverage in your state.

L7368, Lithium ion battery charger, replacement only

HCPCS/CPT

No Prior Auth Required

Code is covered without prior authorization (high confidence)

Medical records must document the beneficiary’s current functional and physical capabilities and the expected functional potential, and must explain differences between current and expected functional states if present.
A clinical evaluation to determine the beneficiary’s functional level must be performed and documented in the medical record.
For fluid/pneumatic/electronic knee coverage for functional level 2, the medical record must document the rationale that the selected knee will improve functional outcomes (e.g., fall reduction), help accomplish ADLs, and that lower-level knee systems were considered and ruled out.
For electronic/microprocessor knee coverage at functional level 2, documentation must show the device is indicated for K2, includes stumble-recovery technology, the beneficiary can perform daily charging, and the beneficiary can understand/respond to error alerts.
For addition L5859, documentation must show an existing microprocessor knee (L5856), K3 functional level, documented spine and/or sound-limb comorbidity impairing hip extension/quadriceps that limits K3 function with microprocessor knee alone, and beneficiary ability to daily charge and respond to alerts.
Clinical justification for advanced foot/knee technologic or design features must be retained in the treating practitioner's or prosthetist's files.

A lower limb prosthesis is covered when the beneficiary is motivated to ambulate.
A lower limb prosthesis is covered when the beneficiary is expected to reach or maintain a defined functional state within a reasonable period of time.
Coverage and component selection are based on a documented functional level (K-level 0–4) determined by the treating practitioner and prosthetist considering past prosthetic use, residual limb status, comorbidities, and the beneficiary’s desire to ambulate.
Foot components L5970 or L5974 are covered for beneficiaries with functional level >=1.
Flexible-keel foot L5972 or multiaxial ankle/foot L5978 are covered for beneficiaries with functional level >=2.
Microprocessor-controlled ankle/foot (L5973), energy storing (L5976), dynamic response multi-axial (L5979), flex foot systems (L5980,L5981), or shank-foot with vertical loading pylon (L5987) are covered when the beneficiary is functional level >=3, or when functional level =2 and the beneficiary meets the level-2 knee coverage criteria and a higher-level foot is required for safe use of the prescribed knee.