FlexPasser™

For atraumatic retrieval of severed flexor tendons with minimal incisions.

The FlexPasser Tendon Retrieval Kit provides a system of single-use instrumentation for the retrieval of the retracted proximal tendon stump(s) during the repair of lacerated digital flexor tendon(s) in the hand.

  • Retrieve retracted tendon end with minimal incisions

  • Reduce the risk of damage to tendon end compared to standard technique*

  • Avoid the need for repeat suturing of the tendon end

Surgery to repair lacerated or severed flexor tendons in the hand can lead to additional trauma to the tendon end or tendon sheath which may cause adhesion post-operatively. This trauma and possible adhesion can reduce the range of movement and impair the outcome of the surgery (1,2,3).

The FlexPasser Tendon Retrieval Kit consists of two components:
• An integrated probe and needle carrier.
• A plastic sleeve for lining the sheath of the severed tendon.

The integrated probe and needle carrier consists of a flexible, elongated device with a smooth, semi-rigid, rounded end. At the other end there is a more flexible section to allow for a curved needle and suture to be transferred through the sheath. There is also a wire loop at this end to which is attached the plastic sleeve. This sleeve allows the probe and needle carrier, and then the tendon to be passed through the tendon sheath from proximal to distal without snagging

INDICATIONS

The FlexPasser Tendon Retrieval Kit is intended for use in the retrieval of the proximal tendon stump(s) during the repair of a lacerated digital flexor tendon(s) in the hand.

HOW DOES IT WORK?

Refer to the animation and surgical technique manual.

ORDER NUMBERS

  • 202-1500 – FlexPasser™ Tendon Retrieval Kit

Features and Benefits

  • For atraumatic retrieval of severed flexor tendons with minimal incisions.
  • Retrieve retracted tendon end with minimal incisions.
  • Reduce the risk of damage to tendon end compared to standard technique*
  • Avoid the need for repeat suturing of the tendon end.

    * Based on cadaver trials

Product Documents

CONTRAINDICATIONS

  • The instrument must not be used for any procedure other than the intended use.

Additional Information

Please note: Regulatory approval for products mentioned on this website varies from country to country. For further information, and for details of local distributors and agents, contact our Sales and Marketing team at enquiries@xirosna.com. All data listed on this page is held at Xiros and can be requested by contacting enquiries@xirosna.com.