PyroCarbon PIP Total Joint
Choosing the PIP Pyrocarbon implant option to limit uncertainty during your PIP replacement cases for young and demanding patients.
Features
- PyroCarbon material with bone friendly, elasticity and durability properties.
- Two cut design for proximal component to preserve collateral ligaments.
- Dorsal notch in distal component to re-insert extensor tendon and preserve natural anatomy.
- Flexible sizing optionsColor coded instrumentation.
Indications
The Ascension Silicone PIP Finger Joint Prosthesis is intended for cementless replacement of the proximal interphalangeal (PIP) joint where disabled by rheumatoid, degenerative, or traumatic arthritis.
Contraindications
- Active local or systemic infection;
- Destruction of the metacarpal, phalanx, or phalanges or poor bone quality which prevents adequate fixation of the implant;
- Loss of musculature, neuromuscular compromise, or vascular deficiency in the affected finger;
- Growing patients with open epiphyses
- Patients with high activity levels; and
- Patients unwilling or unable to comply with physician’s instructions.
Ordering Information
NC
Product Catalogues
Regulatory Information
Class I and IIa and IIb devices.
Ascension Orthopedics, inc.
8700 Cameron road Suite 100
Austin, Texas 78754 • USA
Integra LifeSciences Services (France)
Immeuble Sequoia 2 • 97 allée Alexandre Borodine
Parc technologique de la Porte des Alpes
69800 Saint Priest • FRANCE
Phone: +33 (0)4 37 47 59 00 • fax: +33 (0)4 37 47 59 99
integralife.eu
Legal information
Availability of these products might vary from a given country or region to another, as a result of specific local regulatory approval or clearance requirements for sale in such country or region.
• Consult product labels and inserts for any indications, contraindications, hazards, warnings, precautions and instructions for use.
• Non contractual document. Integra reserves the right, without prior notice, to modify the products in order to improve their quality.
• Warning: Applicable laws restrict these products to sale by or on the order of a physician.
Please contact Integra customer service should you need any additional information on devices classification. All the medical devices mentioned on this document are CE marked according to European council directive 93/42/ EEC on medical devices and its relatives, unless specifically identified as “NOT CE MARKED”.
Integra and the Integra logo are registered trademarks of Integra LifeSciences Corporation or its subsidiaries in the USA and/or other countries. ©2017 Integra LifeSciences Corporation. All rights reserved.
Last modification date: 07/2017. 0491144-2-EN
Document for use in Europe, Middle-East & Africa only.
For complete product information, please consult product labels and inserts for any indications, contraindications, hazards, warnings, precautions, and instructions for use.
