We live in an interconnected and internet-connected world. So, why should our medical devices be any different?
By combining the power of Persona® The Personalized Knee® with CANARY canturio™te with CHIRP™ System, we are proud to introduce the first and only smart implant: Persona IQ.
Smart
Connected
Simple
Privacy
At Zimmer Biomet, we understand the importance of privacy and are dedicated to protecting that right. That’s why we only use customer and patient data to provide the services we’ve agreed upon and for purposes that will enable those services. Persona IQ is not designed to track patient location, and Zimmer Biomet will protect the data you entrust us with through strong safeguards.
Indications
The Canary Tibial Extension (CTE) with Canary Health Implanted Reporting Processor (CHIRP) System is intended to provide objective kinematic data from the implanted medical device during a patient’s total knee arthroplasty (TKA) post-surgical care. The kinematic data are an adjunct to other physiological parameter measurement tools applied or utilized by the physician during the course of patient monitoring and treatment post-surgery.
The device is indicated for use in patients undergoing a cemented TKA procedure that are normally indicated for at least a 58 mm sized tibial stem extension.
The objective kinematic data generated by the CTE with CHIRP System are not intended to support clinical decision-making and have not been shown to provide any clinical benefit.
The CTE with CHIRP System is compatible with Zimmer Persona® Personalized Knee System.
Contraindications
The canturio™ te (CTE) is contraindicated for use in patients who are undergoing procedures or treatments at or in the proximity of the CTE using therapeutic ionizing radiation can result in shortened battery life or premature failure of electronic components. Damage to the CTE by therapeutic ionizing radiation may not be immediately detectable.
Before performing TKA on any patient, consider the following contraindications.
The Zimmer Biomet Persona® Knee System is contraindicated for use in patients who have:
Total Knee Arthroplasty is contraindicated in patients who have rheumatoid arthritis (RA) accompanied by an ulcer of the skin or a history of recurrent breakdown of the skin because their risk of postoperative infection is greater. RA patients using steroids may also have increased risk of infection. Late infections in RA patients have been reported 24+ months postoperative.
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For product information, including indications, contraindications, warnings, precautions, potential adverse effects and patient counseling information, see the package insert or contact your local representative; search this website for additional product information. To obtain a copy of the current Instructions for Use (IFU) for full prescribing and risk information, please visit labeling.zimmerbiomet.com or call 1-800-348-2759, press 4 for 411 Technical Support.
