Primary Device ID | 00817701020219 |
NIH Device Record Key | b43dc7dd-6a08-4e77-ba6b-7fef07b6ebe2 |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | Arcus Staple System |
Version Model Number | ARC-2017K |
Company DUNS | 060783407 |
Company Name | NEXTREMITY SOLUTIONS, INC. |
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 |
Device Issuing Agency | Device ID |
---|---|
GS1 | 00817701020219 [Primary] |
JDR | Staple, Fixation, Bone |
Steralize Prior To Use | false |
Device Is Sterile | true |
Public Version Status | Update |
Device Record Status | Published |
Public Version Number | 4 |
Public Version Date | 2018-07-26 |
Device Publish Date | 2016-09-26 |
00817701020219 | 20mm X 17mm Arcus Staple Kit |
00817701020202 | 16mm X 13mm Arcus Staple Kit |
00817701020196 | 13mm X 10mm Arcus Staple Kit |
00817701020189 | 10mm X 8mm Arcus Staple Kit |
00817701020172 | 8mm X 8mm Arcus Staple Kit |
00817701020165 | 20mm X 17mm Arcus Staple Individual Assembly |
00817701020158 | 16mm X 13mm Arcus Staple Individual Assembly |
00817701020141 | 13mm X 10mm Arcus Staple Individual Assembly |
00817701020134 | 10mm X 8mm Arcus Staple Individual Assembly |
00817701020127 | 8mm X 8mm Arcus Staple Individual Assembly |
00817701020110 | Arcus Staple Sizing Template Kit |