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PRECICE® Intramedullary Limb Lengthening System

An innovative, market-leading solution to help patients with limb length discrepancy (LLD). The PRECICE system is an intramedullary device that once implanted utilizes an External Remote Controller (ERC) to non-invasively lengthen the femur and tibia.

LESS INVASIVE PROCEDURE

STIMULATES AND REGENERATES BONE GROWTH

ELIMINATES EXTERNAL FIXATION1

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About the PRECICE® Intramedullary Limb Lengthening System

0
out of 1,000 children are born with
limb length discrepancy (LLD).
0
minutes a day is all it takes for PRECICE technology to work.2
0+
doctors currently perform PRECICE procedures.

1. Fragomen AT, Rozbruch SR. The mechanics of external fixation. HSS J 2007;3(1):13-29.

2. Paley D. PRECICE intramedullary limb lengthening system. Expert Rev Med Devices 2015;12(3):231-49.

The PRECICE Intramedullary Limb Lengthening (IMLL) System is composed of an implantable intramedullary nail, locking screws, reusable instruments, and a hand-held External Remote Controller (ERC). The PRECICE nail is a sterile single use device that is surgically implanted using the instruments and locking screws. The ERC is used daily after implantation to non-invasively lengthen or shorten the implant to a prescribed length. The PRECICE System is intended for limb lengthening of the femur and tibia. Contraindications include infection or pathologic conditions of bone such as osteopenia which would impair the ability to securely fix the device, metal allergies and sensitivities, patients whose distance from the surface of the treated limb to the intramedullary canal is greater than 51 mm for the 10.7 and 12.5 mm diameter implants or greater than 38 mm for the 8.5 mm diameter implant, patients with an irregular bone diameter that would prevent insertion of the PRECICE nail, patients in which the PRECICE nail would cross joint spaces or open epiphyseal growth plates, patients in which there is an obliterated medullary canal or other conditions that tend to retard healing such as blood supply limitations, peripheral vascular disease or evidence of inadequate vascularity, patients unwilling or incapable of following postoperative care instructions, patients weighing in excess of 114 Kg for the 10.7 and 12.5 mm diameter implants (models A-G, H, J, K, and U) or weighing in excess of 57 Kg for the 8.5 and 10.7 mm diameter implants models (A-G, H, J, K, U, N, M ,P, and Q). The implantable device is only to be used by a trained licensed physician. Please refer to the PRECICE IMLL System instructions for use for complete Important Safety Information. Caution: Federal law restricts this device to sale by or on the order of a physician.