WARSAW, Ind., Sept. 16, 2019 /PRNewswire/ — Zimmer Biomet Holdings, Inc. (NYSE and SIX: ZBH), a global leader in musculoskeletal healthcare, has announced 510(k) clearance from the U.S. Food and Drug Administration (FDA) for the JuggerStitch™ meniscal repair device. The JuggerStitch device is the next generation of this pioneering meniscus repair technology to receive 510(k) clearance and it …