Arthrotek, Inc. - FDA 510(k) Cleared Devices
Recent clearances: ARTHROTEK MAXFIRE MENISCAL REPAIR DEVICE, 2.8 & 3.5MM LACTOSCREW SUTURE ANCHORS, HITCH LACTOSORB SUTURE ANCHOR
17
Total
17
Cleared
0
Denied
FDA 510(k) Regulatory Record - Arthrotek, Inc. Dental ✕
1 devices