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    Cartiva, Inc. Announces First US Procedure for FDA Approved Cartiva Synthetic Cartilage Implant

    Investing News Network
    Jul. 12, 2016 10:53AM PST
    Medical Device Investing

    ALPHARETTA, Ga.–(BUSINESS WIRE)–Cartiva, Inc. announced today that the first commercial U.S. patient has received the Cartiva Synthetic Cartilage Implant (SCI) following its approval by the U.S. Food and Drug Administration (FDA) on July 1. The Cartiva SCI device is intended for use in the treatment of patients with painful arthritis at the base of the …

    ALPHARETTA, Ga.–(BUSINESS WIRE)–Cartiva, Inc. announced today that the first commercial U.S. patient has
    received the Cartiva Synthetic Cartilage Implant (SCI) following its
    approval by the U.S. Food and Drug Administration (FDA) on July 1. The
    Cartiva SCI device is intended for use in the treatment of patients with
    painful arthritis at the base of the big toe, the most common arthritic
    condition in the foot. The outpatient procedure was performed by Dr.
    Judith F. Baumhauer at University of Rochester Medical Center’s Sawgrass
    Surgery Center.
    The first synthetic cartilage device approved by the FDA, Cartiva
    provides another option for millions of patients who suffer from
    arthritis of the big toe joint. The current standard of care involves
    fusing the bones in the arthritic joint with screws and plates. While
    fusion is an effective procedure for eliminating pain, it permanently
    prevents movement of the joint. During the Cartiva procedure, the
    damaged cartilage is removed and replaced with Cartiva SCI, a
    biocompatible, biomedical polymer implant, providing a cartilage-like,
    compressible, low-friction and durable bearing surface. Unlike a fusion
    procedure, patients may begin weight bearing immediately as tolerated.
    “Today, one in 40 Americans over the age of 50 experience arthritis of
    the toe, and with the aging population, that number is likely to grow.
    This condition can be particularly life-impacting – limiting a person’s
    ability to conduct functional activities of daily living, producing pain
    and discomfort and restricting shoe wear options,” said Dr. Baumhauer.
    “The Cartiva implant was accomplished in a quick, simple surgical
    procedure and we look forward to offering this innovative option to more
    people in need.”
    About Cartiva, Inc.
    Based in Alpharetta, Ga., Cartiva, Inc. develops and markets innovative
    solutions for patients with cartilage damage and osteoarthritis.
    Cartiva’s venture investors include New Enterprise Associates, Windham
    Venture Partners and Domain Associates. Additional information is
    available on the company’s website at www.cartiva.net.

    food and drug administration
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