Arthrosurface receives FDA 510(k) clearance for KISSloc Suture System

Arthrosurface received 510(k) clearance from the U.S. Food and Drug administration for the KISSloc Suture System.

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The system is a mini plate and suture implant intended for the correction of a Hallux Valgus deformity, universally known as a bunion. It is sterile packaged with completely disposable instrumentation.

Arthrosurface focuses on the design and distribution of orthopedic devices for joint preservation, restoration and resurfacing.

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