Disclaimer: This site aggregates publicly available data from official government sources (FDA, ClinicalTrials.gov, PubMed, SEC EDGAR) for general reference only. It does NOT constitute medical advice, diagnosis, treatment recommendations, or investment advice.

Arthrosurface, Inc.

FDA 510(k) & PMA Approved Devices — 11 products

Total Devices11
Categories8
Latest FDA decision2021-06-24
TypeNumberDevice NameCodeDateActions
510(k) K203375 OVOMotion Reverse Shoulder Arthroplasty SystemPHX2021-06-24 View
510(k) K200718 Arthrosurface WristMotion Total Wrist Arthroplasty SystemJWJ2020-10-15 View
510(k) K190261 BOSS Toe Fixation SystemKWD2019-08-14 View
510(k) K181280 Patello-Femoral Wave (Kahuna) Arthroplasty SystemKRR2018-06-14 View
510(k) K173964 OVOMotion Shoulder Arthroplasty SystemHSD2018-04-18 View
510(k) K172383 Arthrosurface Bone ScrewsHWC2017-12-22 View
510(k) K170440 KISSloc Suture SystemHTN2017-05-03 View
510(k) K170350 ToeMATE® Hammertoe Correction SystemHWC2017-03-03 View
510(k) K162391 AlignMATE™ Lapidus Arthrodesis SystemHRS2017-02-21 View
510(k) K161539 Arthrosurface Bone ScrewsHWC2016-06-30 View
510(k) K152454 HemiCAP MTP Resurfacing Hemi-Arthroplasty SystemKWD2016-04-11 View
↑