Wrightmedicaltechnologyinc

FDA Regulatory Profile

Summary

Total Recalls
0
510(k) Clearances
302
Inspections
0
Compliance Actions
0

Recent 510(k) Clearances

K-NumberDeviceDate
K222835Prophecy Preoperative Navigation Alignment SystemJanuary 27, 2023
K213342PRO-DENSE LoVisc Bone Graft SubstituteJanuary 5, 2022
K212996Sterile PHALINX Hammertoe SystemNovember 16, 2021
K202815PROPHECY Preoperative Navigation Alignment SystemMarch 10, 2021
K201259ORTHOLOC 2 with 3Di Technology Pilon Fracture Plating SystemJanuary 8, 2021
K200507PRO-DENSE LoVisc Bone Graft SubstituteOctober 21, 2020
K193067The INBONE™ Total Ankle System, the INFINITY™ Total Ankle System and the INVISION™ Total Ankle RevisJune 8, 2020
K191393INFINITY Total Ankle System, INBONE Total Ankle SystemAugust 22, 2019
K190970PROSTEP™ TBI™ (Tailors Bunion Implant) SystemAugust 13, 2019
K183620PROSTEP TBC Implant SystemJune 6, 2019
K190482IGNITE Bone Void FillerMay 28, 2019
K190670ORTHOLOC™ 2 Lapidus with Rotation SystemMay 14, 2019
K190283PROSTIM Injectable Inductive GraftMarch 14, 2019
K183026Wright Jones Fracture SystemMarch 13, 2019
K181377PROSTEP MICA Screw SystemJanuary 11, 2019
K182823PRODENSE Bone Graft SubstituteNovember 2, 2018
K181255PRODENSE Bone Graft SubstituteSeptember 12, 2018
K181557INFINITY Total Ankle SystemAugust 9, 2018
K180730INVISION Total Ankle Revision SystemJuly 11, 2018
K180024SALVATION Midfoot NailJuly 11, 2018