OrthoLimited
peek anchor
OrthoLimited

PEEK Anchor

PEEK Anchor — a orthopedic device from OrthoLimited, supplied to ISO 13485 standards for hospitals and distributors worldwide.

MPN
C001
Brand
OrthoLimited
Manufactured by
OrthoLimited Inc.
Warehouse
EU
Availability
In stock
  • âś“ CE marked
  • âś“ ISO 13485
  • âś“ Warranty included
  • âś“ Worldwide shipping
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Regulatory: For professional surgical use only. Availability and certification vary by country; confirm local regulatory status before purchase or use.

Clinical overview

Product overview

What is an anchoring suture?

, tendons, ligaments, and meniscus) to the bone and have become essential devices in sports medicine and during arthroscopic surgery. As the usage of suture anchors has increased, various material-specific advantages and challenges have been reported. As a result, suture anchors are continually changing to become safer and more efficient.

In this ever-changing environment, it is clinically essential for the surgeon to understand the key characteristics of existing anchors sufficiently.

) Shoulder surgery particularly has experienced a significant change in the type of techniques used from open repair of the rotator cuff and labrum using screws, washers, transosseous sutures, and staples to arthroscopic repair using suture anchors.

The primary function of the suture anchor is to attach tissue at the proper site and maintain its position without loosening or excessive tension until physiologic healing is accomplished. ) Various types of anchors have been developed, and designs of anchors have evolved over the recent decade to maximize their effectiveness in creating a firm tendon-to-bone repair.

Polyetheretherketone

Because some biodegradable anchors can be absorbed too quickly, the development of biostable anchors was pursued. Such a biostable anchor—a polyetheretherketone (PEEK) polymer—is obtained by dialkylation of bisphenol salts )

PEEK is increasingly becoming used in tribological components because of its excellent performance. PEEK materials showed high strength, strong mechanical properties, good wear- and heat-resistance, and excellent chemical and biological resistance. ) PEEK also offers advantages, such as good postoperative imaging and stable fixation, and no complications associated with polymer degradation.

Importantly, the major problem with PEEK has been shown to be poor osseointegration. .)

BIOCOMPOSITE SUTURE ANCHOR

Biocomposite suture anchors are composed of both a biodegradable polymer material and a bone formation-promoting bioceramic material. ) TCP is widely used in orthopedic surgery to fill bone defects because (1) it has a mineral content similar to that of human bone, (2) its macro-porosity and micro-porosity is osteoconductive, and (3) it has excellent biocompatibility and mechanical resistance. ) Generally, hydroxyapatite-based bone substitute materials are considered nonabsorbable or have much lower degradation rates than β-TCP (Fig.

3))

ALL-SOFT SUTURE ANCHOR

Solid type suture anchors (e.g., metal and polymer) have been studied extensively and found to be sufficient for maintaining physiologic loads at soft tissue to bone junctions. Usually, these solid type anchors need surgical preparation of the bony footprint site (decortication, punching, or drilling) that may cause bone loss because of the grounding piece's volume.)

All-soft suture anchors (ASAs) were developed to minimize complications and invasiveness related to the use of solid type anchors. These ASAs consist of one or more ultra-high-molecular-weight polyethylene (UHMWPE)-containing sutures.

The ASAs typically consist of a sleeve or tape made of suture material through which the UHMWPE-containing suture is woven. This fixation mechanism differs compared with screw-type suture anchors. When the ASA is inserted into the bone and the primary suture is pulled, the sleeve or tape is cinched up to compress against the overlying cortical bone creating a “ball” that works as the anchor.

It allows the suture anchor to be placed in a tunnel with a smaller diameter (1–3 mm), thereby preserving bone and hypothetically allowing for more bone preservation, which may be particularly beneficial due to limited bone stock at the glenoid rim or acetabulum. .)

Technical specifications

Engineering at a glance

Documentation, IFU and DOCs available on request — contact our sales team for the full regulatory file.

Model
C001
Material
medical stainless steel
Certification
CE, ISO 9001, ISO 13485

Documents & downloads

Regulatory paperwork & manuals

Pre-cleared documentation for this device. Full tender-pack originals are available on request.

Documents & downloads

Regulatory paperwork & manuals

This device's IFU, CE Declaration of Conformity, ISO 13485 certificate and (where applicable) FDA 510(k) clearance ship with the order. Reach out below for the pack ahead of purchase.

Get in touch

Need configuration help, certificates, or volume pricing?

Our clinical sales team will scope quantities, voltage, accessories and regulatory paperwork — usually within one business day.

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