Tactoset Injectable Bone Substitute Now FDA Cleared for Hardware Augmentation - Seite 2

Dr. Misty Suri, MD from Ochsner Health in New Orleans said, “I am pleased to see the expanded indications for Tactoset cleared for use to augment hardware and bone fragments during surgical procedures. Bone quality is a critical factor when placing load bearing anchors, and the area in which hardware is normally placed is often weaker due to inferior bone quality or insufficiency fractures. Fundamentally, shoulders, knees and other joints that require surgery are often associated with either osteoporotic bone and/or lower quality bone, which significantly increases the potential for pain, hardware failure, and inferior patient outcomes. With this expanded Tactoset indication, we are now able to address the concern for microfractures and bone quality while creating a strong foundation to augment the use of suture anchors and other hardware. This gives surgeons more confidence in repairs such as rotator cuff, shoulder instability, and knee reconstructive surgeries.”

Anika expects to begin actively marketing the expanded indication for Tactoset for hardware augmentation in October 2021.

^{1. Preclinical data on file. Results may not correlate to clinical performance.}

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