- Status Complete
- Type Re-application
- Pre-PASC consultation Closed
- Pre-MSAC consultation Closed
- Outcome Not supported
Application details
Reason for application
Referral from Prostheses List Advisory Committee
Service or technology in this application
Insertion of a bioinductive collagen implant (REGENETEN), to induce formation of new tendon-like tissue that biologically augments the degenerated rotator cuff tendon. The physical and chemical properties of the scaffold provide a layer of collagen between a flat tendon and surrounding tissue, permitting collagen in-growth into the scaffold, and promoting collagen re-modelling with alignment of the collagen fibres in the direction of the stress in the tendon. The scaffold is hydrated in saline and positioned arthroscopically through a small incision over the tendon, with one end overlapping the tendon insertion.
Type: Therapeutic technology
Medical condition this application addresses
A rotator cuff tear is the partial or full detachment of the tendon that attaches the muscles from the shoulder blade to the head of the humerus. The cause of the tear is multifactorial and likely a combination of age-related chronic degeneration of the tendon, direct micro/macro trauma, impingement and/or repetitive or vigorous overhead activity of the arm.
Previous applications
Application documents
Application summary
PICO set
Consultation survey
PICO confirmation
Public summary document
Consultation survey
PICO confirmation
Public summary document
Public summary document
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Consultation survey and deadlines
- PASC consultation: Closed
- MSAC consultation: Closed Friday 14 June 2024
Meetings to consider this application
- PASC meeting: 10 to 11 August 2023
- ESC meeting: 13 to 14 June 2024
- MSAC meeting: 1 to 2 August 2024