Stryker Receives FDA 510(K) Clearance for Shapematch; Cutting Guides

Stryker Orthopaedics, a division of Stryker Corporation SYK, today announced that its ShapeMatch Cutting Guides have been granted 510(k) market clearance by the U.S. Food and Drug Administration for use with the company's Triathlon Total Knee System. The single-use ShapeMatch Cutting Guides are designed and manufactured from patient-specific 3D imaging data that is derived from MRI or CT scans.