Thicker, completely microporous prosthetic material (over 1.0 mm) may compromise full engagement of the tack. Material thickness should be carefully evaluated prior to application. A minimum thickness of tissue over underlying bone, vessels, or viscera is needed for full engagement of the tack. The total distance from the surface of the tissue (including the material to be fixated) to the underlying bone, vessels, or viscera should be carefully evaluated prior to application of the device. Please refer to the tack specification chart for shaft length.
Adverse reactions include seroma, bleeding/hematoma, recurrence, chronic pain, infection, allergic reactions, inflammatory reaction, visceral adhesions, nerve entrapment, and/or damage to pericardium, nerve damage, vascular injury, visceral injuries, injuries to operator, or inadvertent injuries to other tissues that tacks penetrate through.
Please refer to the indications for use (IFU) for complete contraindication and risk information.
Find more information, including other available configurations, for AbsorbaTack™ fixation device.
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