ComposiTCP™ Suture Anchors

The ComposiTCP Suture Anchor is Zimmer Biomet’s first biocomposite, absorbable suture anchor system for securing soft tissue to bone. Made of DuoSorb®, a proprietary biocomposite material blend, these anchors offer strong fixation and a versatile anchor offering.

ComposiTCP-QuattroLink_doubleRow_shoulder-inset
  • Osteoconductive1
  • Pull out strength of 267N2 in sawbone testing
  • Versatile configurations loaded with MaxBraid Suture & BroadBand Suture Tape

Osteoconductive, Biocompatible, and Absorbable1

Material made of 30% β-Tricalcium-Phoshpate (β-TCP), 70% Polylactic Acid (PLDL) mix is a balance of strength and elasticity similar to cortical bone1

  • β-TCP is designed to provide a scaffold for bone ingrowth
  • Higher β-TCP content has shown to limit inflammatory responses in an animal study1
  • ComposiTCP Suture Anchors are gradually replaced by newly formed bone and have shown to absorb over time in an animal study1

Strong Fixation and Easy Insertion in Bone

Reliability in bone makes anchors suitable for medial row use in double row or single row repair

  • The 4.5mm ComposiTCP suture anchor shows a higher average fixation strength of 267N when compared to Arthrex’s 4.5 mm BioComposite Corkscrew® FT suture anchor with 246N in testing2
ComposiTCP_Family-inset

Various Assortments of Suture and Tape Configurations

This anchor platform offers a variety of sizes loaded with #2 round suture in double and triple loaded options and double loaded BroadBand Tape variations

  • The dual channel eyelet design allows for smooth suture sliding and expedited suture management across all platforms
  • Seamless loading into instrumentation with 1.5 mm BroadBand Tape (flat) transition into #2 MaxBraid Suture ends (round)

Additional Information

  1. Aunoble S, Clement Dl, Frayssinet P, et al.Biological performance of a new β-TCP/PLLA composite material forapplications in spine surgery: In vitro and in vivo studies. J Biomed Mater Res. 2006; 78A:416-422. Animal testing data is not necessarily indicative of clinical outcome.
  2. Data on File, SBM. Project No. 867, PR 2002.03. Insertion and pullout tests for standard (knotted) and knotless shoulder implants. 2018.  Laboratory data is not necessarily indicative of clinical outcome.

 

Duosorb® is a trademark of SBM SAS.

Corkscrew® is a trademark of Arthrex, Inc.

 

Legal Manufacturer:                      

SBM SAS
Z.I du Monge
65100 LOURDES
France

 

Distributor:

Biomet Sports Medicine
56 East Bell Drive
P.O. Box 587
Warsaw, Indiana 46581
USA

 


All content herein is protected by copyright, trademarks and other intellectual property rights, as applicable, owned by or licensed to Zimmer Biomet or its affiliates unless otherwise indicated, and must not be redistributed, duplicated or disclosed, in whole or in part, without the express written consent of Zimmer Biomet.  
This material is intended for health care professionals.  Distribution to any other recipient is prohibited.
For product information, including indications, contraindications, warnings, precautions, potential adverse effects and patient counseling information, see the package insert and information on this website. To obtain a copy of the current Instructions for Use (IFU) for full prescribing and risk information, please call 1-800-348-2759, press 4 for 411 Technical Support.