Arthrosurface, Inc. is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Arthrosurface, Inc. - FDA 510(k) Cleared Devices
Recent clearances: OVOMotion Reverse Shoulder Arthroplasty System, Arthrosurface WristMotion Total Wrist Arthroplasty System, BOSS Toe Fixation System
26
Total
26
Cleared
0
Denied
Arthrosurface, Inc. has 26 FDA 510(k) cleared orthopedic devices. Based in Stoughton, US.
Last cleared in 2021. Active since 2004.
Browse the complete list of FDA 510(k) cleared orthopedic devices from this manufacturer. Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Arthrosurface, Inc.
26 devices
Cleared
Jun 24, 2021
OVOMotion Reverse Shoulder Arthroplasty System
Orthopedic
220d
Cleared
Oct 15, 2020
Arthrosurface WristMotion Total Wrist Arthroplasty System
Orthopedic
210d
Cleared
Aug 14, 2019
BOSS Toe Fixation System
Orthopedic
187d
Cleared
Jun 14, 2018
Patello-Femoral Wave (Kahuna) Arthroplasty System
Orthopedic
30d
Cleared
Apr 18, 2018
OVOMotion Shoulder Arthroplasty System
Orthopedic
110d
Cleared
Dec 22, 2017
Arthrosurface Bone Screws
Orthopedic
136d
Cleared
May 03, 2017
KISSloc Suture System
Orthopedic
78d
Cleared
Mar 03, 2017
ToeMATE® Hammertoe Correction System
Orthopedic
28d
Cleared
Feb 21, 2017
AlignMATE™ Lapidus Arthrodesis System
Orthopedic
179d
Cleared
Jun 30, 2016
Arthrosurface Bone Screws
Orthopedic
27d
Cleared
Apr 11, 2016
HemiCAP MTP Resurfacing Hemi-Arthroplasty System
Orthopedic
227d
Cleared
Dec 23, 2014
Wrist Hemiarthroplasty System
Orthopedic
160d