The Vanguard XP Total Knee System,
supporting instrumentation platform, and surgical
technique have been designed in collaboration
with the Vanguard XP Development Team:
Prof. Tom Andriacchi
Dr. Keith Berend
Dr. Jeffrey DeClaire
Dr. Craig Della Valle
Dr. Jorge Galante
Dr. Adolph Lombardi
Dr. Chris Peters
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INDICATIONS
1. Painful and disabled knee joint resulting from
osteoarthritis, rheumatoid arthritis or traumatic arthritis
where one or more compartments are involved.
2. Correction of varus, valgus, or post-traumatic
deformity.
3. Correction or revision of unsuccessful osteotomy,
arthrodesis, or failure of previous joint replacement
procedure.
Femoral components and tibial tray components
with porous coatings are indicated for cemented and
uncemented biological fixation application. Non-
coated (Interlok) femoral components, tibial tray
components and all polyethylene patellar components
are indicated for cemented application only. Regenerex
components (where available) are intended only for
uncemented, biologic fixation application.
CONTRAINDICATIONS
Absolute contraindications include: infection, sepsis, and
osteomyelitis. Relative contraindications include:
1) an uncooperative patient or a patient with neurologic
disorders who is incapable of following directions, 2)
osteoporosis, 3) metabolic disorders which may impair
bone formation, 4) osteomalacia, 5) distant foci of
infections which may spread to the implant site, 6) rapid
joint destruction, marked bone loss or bone resorption
apparent on roent genogram, 7) vascular insufficiency,
muscular atrophy, neuromuscular disease, and/or
8) incomplete or deficient soft tissue surrounding the
knee.
For complete product information, including warnings, precautions, and potential adverse effects,
see the package insert and www.Biomet.com (where available). Check for country product clearances
and reference product specific instructions for use.
Summary of Contents for VANGUARD XP
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