Maxon™ and Maxon™ CV sutures are indicated for use as absorbable sutures in general soft tissue approximation and/or ligation, in pediatric cardiovascular tissue, where growth is expected to occur, and in peripheral vascular tissue.
Maxon™ and Maxon™ CV synthetic absorbable sutures elicit a minimal acute inflammatory reaction in tissues, which is followed by gradual encapsulation of the suture by fibrous connective tissue. Progressive loss of tensile strength and eventual absorption of Maxon™ and Maxon™ CV synthetic absorbable sutures occurs by means of hydrolysis where the suture is broken down and subsequently absorbed and metabolized by the body.
Studies indicate that tensile strength for Maxon™ and Maxon™ CV sutures is approximately 80% of the original suture strength at one week post implant. Approximately 75% of the original suture strength remains at two weeks, 65% at three weeks, 50% at four weeks, and 25% at six weeks post-implant. Absorption of Maxon™ and Maxon™ CV synthetic absorbable sutures is minimal until about the sixtieth day after implantation. Absorption is substantially complete within six months.
Find more information, including other available configurations, for Maxon™ monofilament absorbable suture.
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