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Contraindications - DePuy Mitek HEALIX ADVANCE KNOTLESS Bedienungsanleitung

Suture anchor
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  • DEUTSCH, seite 17
(PDS
) and un-dyed non-absorbable polyethylene.
®
The partially absorbable suture is coated with a
copolymer of 90% caprolactone and 10% glycolide.
INDICATIONS
The HEALIX ADVANCE KNOTLESS Anchors are
indicated for use in the following procedures for
reattachment of soft tissue to bone:
Indication
Rotator Cuff
Biceps Tenodesis

CONTRAINDICATIONS

• Procedures other than those listed in the
INDICATIONS section.
• Pathologic conditions of bone such as cystic
changes or severe osteopenia that would impair
its ability to securely fix the HEALIX ADVANCE
KNOTLESS Anchors.
• Pathologic changes in the soft tissues being fixated
to bone that would prevent their secure fixation by
the HEALIX ADVANCE KNOTLESS Anchors.
• Comminuted bone surface that would militate
against secure fixation of the HEALIX ADVANCE
KNOTLESS Anchors.
• Physical conditions that would eliminate or tend
to eliminate adequate implant support or retard
healing, i.e., blood supply limitation, previous
infection, etc.
• Conditions which tend to limit the patient's ability
to restrict activities or follow directions during the
healing period.
• The HEALIX ADVANCE KNOTLESS Anchors are
not designed for and should never be used to attach
artificial ligaments.
PRECAUTIONS
• The HEALIX ADVANCE KNOTLESS Anchors are
supplied STERILE, and are intended for single
use only. Do not re-sterilize. Do not use if sterile
packaging appears to be damaged.
• The product should be stored under cool, dry
conditions.
Implant Material
PEEK
X
X
2
BR
X
X

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