ADVANSYS®
Integra News
Integra Events
Transparence

Loi Bertrand
Professionnels de santé exerçant en France, veuillez consulter la page Bienvenue.

ADVANSYS®

Limit uncertainty with…

ADVANSYS® Dorsal Lisfranc Plate
The Dorsal Lisfranc Plates are intended for fractures, fusions, osteotomies and replantations of small bones at the tarso-metatarsal joints (Lisfranc joints).

  • 3 sizes of implants: 3 right & 3 left plates (small, medium and large).
  • 3.5 mm diameter screws available in lengths from 8 mm to 34 mm in 2 mm increments.
  • 3.5 mm lock-screws.

ADVANSYS® Medial Lisfranc Plate
The Medial Lisfranc Plates are intended to be used for bone fixation such as:

  • Lisfranc arthrodesis.
  • Mono or bi-cortical osteotomies or fractures near the 1st metatarso-cuneiform joint.
  • 2 sizes of implants: 2 right & 2 left plates (small and large sizes).
  • 3.5 mm diameter screws available in lengths from 8 mm to 34 mm in 2 mm increments.
  • 3.5 mm lock-screws.

ADVANSYS® TTC Fusion Plate
The TTC Plates are intended for arthrodesis of the ankle joint and calcanea, osteotomies, fusions and replantations of small bones in the ankle and distal tibia.

  • 4 sizes of implants.
  • 4 right & 4 left plates (in 6,7,8,9 holes configurations).
  • Screw dia.4.5 mm for fixation of the tibia and talus – Length 14 mm to 65 mm.
  • Screw dia.6.5 mm for fixation of the calcaneus – Length 20 mm to 65 mm.
  • Lock-screws for 4.5 mm dia. screws.
  • Lock-screws for 6.5 mm dia. screws.

Indications

The TTC plate are intended for arthrodesis of the ankle joint and distal tibia, fractures, osteotomies, fusions and replantations of small bones in the foot and ankle.

Contraindications

The implant should not be used in a patient who has currently, or who has a history of :

  • Intact asymptomatic subtalar joint.
  • Active local or systemic infection.
  • Severe peripheral vascular disease.
  • Severe longitudinal deformity.
  • Insufficient quantity or quality of bone to permit stabilization of the arthrodesis.
  • Conditions that restrict the patient’s ability or willingness to follow postoperative instructions during the healing process.
  • Suspected or documented metal allergy or intolerance.

Ordering Information

NC


Product Catalogues


Regulatory and Legal Information

For more information, please contact your Integra representative.
For complete product information, please see the Instructions for Use accompanying each product.