Medical Device Manufacturer · US , Stoughton , MA

Arthrosurface, Inc. - FDA 510(k) Cleared Devices

26 submissions · 26 cleared · Since 2004
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
1-12 of 26
Cleared Jun 24, 2021
OVOMotion Reverse Shoulder Arthroplasty System
K203375 · PHX
Orthopedic · 220d
Cleared Oct 15, 2020
Arthrosurface WristMotion Total Wrist Arthroplasty System
K200718 · JWJ
Orthopedic · 210d
Cleared Aug 14, 2019
BOSS Toe Fixation System
K190261 · KWD
Orthopedic · 187d
Cleared Jun 14, 2018
Patello-Femoral Wave (Kahuna) Arthroplasty System
K181280 · KRR
Orthopedic · 30d
Cleared Apr 18, 2018
OVOMotion Shoulder Arthroplasty System
K173964 · HSD
Orthopedic · 110d
Cleared Dec 22, 2017
Arthrosurface Bone Screws
K172383 · HWC
Orthopedic · 136d
Cleared May 03, 2017
KISSloc Suture System
K170440 · HTN
Orthopedic · 78d
Cleared Mar 03, 2017
ToeMATE® Hammertoe Correction System
K170350 · HWC
Orthopedic · 28d
Cleared Feb 21, 2017
AlignMATE™ Lapidus Arthrodesis System
K162391 · HRS
Orthopedic · 179d
Cleared Jun 30, 2016
Arthrosurface Bone Screws
K161539 · HWC
Orthopedic · 27d
Cleared Apr 11, 2016
HemiCAP MTP Resurfacing Hemi-Arthroplasty System
K152454 · KWD
Orthopedic · 227d
Cleared Dec 23, 2014
Wrist Hemiarthroplasty System
K141920 · KWN
Orthopedic · 160d
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