Primary Device ID | M5288W152223W0 |
NIH Device Record Key | 573034ef-61e6-4fdd-a83e-5e5f1e224ad2 |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | WristMotion® Wrist Hemiarthroplasty System |
Version Model Number | 8W15-2223-W |
Catalog Number | 8W15-2223-W |
Company DUNS | 144666109 |
Company Name | ARTHROSURFACE INCORPORATED |
Device Count | 1 |
DM Exempt | false |
Pre-market Exempt | false |
MRI Safety Status | Labeling does not contain MRI Safety Information |
Human Cell/Tissue Product | false |
Device Kit | false |
Device Combination Product | false |
Single Use | true |
Lot Batch | true |
Serial Number | false |
Manufacturing Date | true |
Expiration Date | true |
Donation Id Number | false |
Contains Natural Rubber Latex | false |
Labeled No Natural Rubber Latex | false |
RX Perscription | true |
OTC Over-The-Counter | false |
Phone | 508-520-3003 |
contact@arthrosurface.com |
Device Issuing Agency | Device ID |
---|---|
HIBCC | M5288W152223W0 [Primary] |
KWN | Prosthesis, Wrist, Carpal Lunate |
Steralize Prior To Use | false |
Device Is Sterile | true |
Public Version Status | New |
Device Record Status | Published |
Public Version Number | 1 |
Public Version Date | 2020-04-08 |
Device Publish Date | 2020-03-31 |
M5288W950016W0 | Taper Post, 7.5mm Dia, Capitate, CE |
M5288W153523W0 | 15mm Capitate Component, 35mm x 23mm, Wrist, CE |
M5288W153517W0 | 15mm Capitate Component, 35mm x 17mm, Wrist, CE |
M5288W152223W0 | 15mm Capitate Component, 22mm x 23mm, Wrist, CE |
M5288W152217W0 | 15mm Capitate Component, 22mm x 17mm, Wrist, CE |
M5288W123517W0 | 12mm Capitate Component, 35mm x 17mm, Wrist, CE |
M5288W122217W0 | 12mm Capitate Component, 22mm x 17mm, Wrist, CE |
Mark Image Registration | Serial | Company Trademark Application Date |
---|---|
WRISTMOTION 86513724 5551113 Live/Registered |
ARTHROSURFACE INCORPORATED 2015-01-26 |
WRISTMOTION 86513709 5079866 Live/Registered |
ARTHROSURFACE INCORPORATED 2015-01-26 |