Primary Device ID | M528G2032515W0 |
NIH Device Record Key | fb64677c-07d0-4508-be75-ab39e2ca7013 |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | HemiCAPGRS® |
Version Model Number | G203-2515-W |
Catalog Number | G203-2515-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 | false |
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 | M528G2032515W0 [Primary] |
KWS | Prosthesis, Shoulder, Semi-Constrained, Metal/Polymer Cemented |
Steralize Prior To Use | false |
Device Is Sterile | true |
Public Version Status | Update |
Device Record Status | Published |
Public Version Number | 4 |
Public Version Date | 2019-12-23 |
Device Publish Date | 2015-09-15 |
M528G2032520W0 | ARTICULAR, 20 X 25MM IMPLANT, GLENOID 53/50 HEAD |
M528G2032520A0 | ARTICULAR, 20 X 25MM IMPLANT, GLENOID 53/50 HEAD |
M528G2032515W0 | ARTICULAR, 20 x 25mm IMPLANT, GLENOID 58/55 HEAD |
M528G2032515A0 | ARTICULAR, 20 x 25mm IMPLANT, GLENOID 58/55 HEAD |
M528G2032015W0 | ARTICULAR, 19 x 20mm IMPLANT, GLENOID 53/50 HEAD |
M528G2032015A0 | ARTICULAR, 19 x 20mm IMPLANT, GLENOID 53/50 HEAD |
M528G2032010W0 | ARTICULAR, 19 x 20mm IMPLANT, GLENOID 58/55 HEAD |
M528G2032010A0 | ARTICULAR, 19 x 20mm IMPLANT, GLENOID 58/55 HEAD |
M528G00714000 | Glenoid Pin Kit |
M528G00002000 | Glenoid Universal Delivery Kit-Twin Glenoid |
M528G00001000 | Glenoid Universal Delivery Kit |