| PANTA™
Arthrodesis Nail - Indications for Use |
|
Indications for Use
The PANTA™ Arthrodesis Nail is intended for use
in tibio-talo-calcaneal arthrodesis including deformities
of the hindfoot and the distal tibia. Depending on the
particular patient factors, indications
may include:
- Post-traumatic and degenerative arthritis involving
both ankle and subtalar joints
- Rheumatoid arthritis
- Revision of failed ankle arthrodesis with subtalar
involvement or with an insufficient talar body
- Revision of failed total ankle arthroplasty with subtalar
intrusion
- Talar deficiency conditions requiring tibiocalcaneal
arthrodesis
- Avascular necrosis of the talus
- Neuroarthropathy or neuropathic ankle deformity
- Severe deformity as a result of talipes equinovarus,
cerebral vascular accident, paralysis or other neuromuscular
disease
- Severe pilon fractures with trauma to the subtalar
joint
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
- Obliterated medullary canal or otherconditions which
tend to retard healing such as blood supply limitations,
previous infections
- Conditions that restrict the patient's ability or
willingness to follow postoperative instructions during
the healing process
- Insufficient plantar pad
- Suspected or documented metal allergy or intolerance
