,for, Item ID-
  • #831249
  • J & J Healthcare Systems #SXPD2B403

Absorbable Suture with Needle STRATAFIX™ Bidirectional Knotless Tissue Control Device Spiral PDO CT-1 1/2 Circle Taper Point Needle Size 1 Monofilament

SUTURE, SPIRAL PDO 1-0 30CM 36MM 1/2" CIR (12/BX)

Features

  • With significantly more points of fixation than traditional sutures, STRATAFIX™ devices give surgeons more consistent control over every pass and combine the strength and security of interrupted closure with more efficiency than continuous closure
  • STRATAFIX™ Spiral PDO Knotless Tissue Control Device consists of barbed suture material, armed with a surgical needle on each end
  • Barbs allow for tissue approximation without the need to tie surgical knots
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Product Specifications


Features
  • With significantly more points of fixation than traditional sutures, STRATAFIX™ devices give surgeons more consistent control over every pass and combine the strength and security of interrupted closure with more efficiency than continuous closure
  • STRATAFIX™ Spiral PDO Knotless Tissue Control Device consists of barbed suture material, armed with a surgical needle on each end
  • Barbs allow for tissue approximation without the need to tie surgical knots
  • STRATAFIX™ Spiral PDO Device is comprised of dyed (violet) polyester, poly (p-dioxanone)
  • The strength of the Stratafix device can be compared to USP knot strength of non-barbed sutures
  • Absorption of STRATAFIX PDO Device is minimal until about 120 days, and is essentially complete within 180 days (six months)
  • STRATAFIX™ Spiral PDO Device contains bidirectionally oriented barbs to anchor tissues and does not require knots to approximate opposing edges of a wound
  • Tying knots on the barbed section of the material will damage the barbs and potentially reduce the suture tensile strength and barb effectiveness
  • For the bidirectional forces to be created and for the device to function properly, both sides of the STRATFIX device must be engaged in the tissue
  • Additionally, when completing placement, an additional backstitch or bite of tissue lateral to the end of the incision is required to lock the device in place
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