LCDActive
Amniotic and Placental-Derived Product Injections and/or Applications for Musculoskeletal Indications, Non-Wound
L39116
Effective: October 23, 2025
Updated: December 31, 2025
Policy Summary
This policy states that injections and/or applications of any amniotic or placental-derived products for musculoskeletal indications (including tendon/ligament injuries, cartilage damage, osteoarthritis, joint/back pain, and adjunctive orthopedic uses) are not covered. The policy does not address burns, wounds, or ophthalmic uses, and cites limited standardization and insufficient human safety/efficacy evidence plus variable FDA regulatory status as the rationale.
Coverage Criteria Preview
Key requirements from the full policy
"Amniotic membrane, amniotic fluid, or any other placental-derived product injections and/or applications for musculoskeletal injuries, joint conditions, or other musculoskeletal indications are not..."
Sign up to see full coverage criteria, indications, and limitations.