Winter Innovations Receives FDA 510(k) Clearance and PCCP Authorization for Expanded EasyWhip® Family
Knoxville, TN – Winter Innovations, Inc. a medical device company developing innovative solutions for orthopedic soft tissue surgery, announced today that the U.S. Food and Drug Administration (FDA) has granted 510(k) clearance for the expanded EasyWhip® Family.
The EasyWhip® Family builds on Winter Innovations’ flagship EasyWhip® technology, a two-part needle system designed to facilitate easy, fast, and accurate stitch placement with less variation in orthopedic ligament and tendon surgeries. The clearance covers six additional EasyWhip® products across a range of suture sizes and needle geometries, including new curved variants.
EasyWhip® enables surgeons to create both traditional whip stitches and Winter Innovations’ proprietary WhipLock™ stitch pattern with a single device. By offering additional suture sizes and needle configurations, the EasyWhip® Family is designed to meet a broader range of procedural needs and surgeon preferences across sports medicine, foot and ankle, and other orthopedic soft tissue procedures.
