Primary Device ID | 00816988012665 |
NIH Device Record Key | fb12f193-b6ac-4eea-91ab-108eba0016fa |
Commercial Distribution Discontinuation | 2020-07-07 |
Commercial Distribution Status | Not in Commercial Distribution |
Brand Name | Sonoma Orthopedic Products, Inc. |
Version Model Number | 3.0mm x 47mm Jones Bolt |
Catalog Number | 5MT53047 |
Company DUNS | 131747628 |
Company Name | ARTHREX, 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 | 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 |
Device Issuing Agency | Device ID |
---|---|
GS1 | 00816988012665 [Primary] |
HSB | Rod, Fixation, Intramedullary And Accessories |
Steralize Prior To Use | false |
Device Is Sterile | true |
Public Version Status | Update |
Device Record Status | Published |
Public Version Number | 3 |
Public Version Date | 2020-07-08 |
Device Publish Date | 2017-04-04 |
00888867430341 - Arthrex® | 2024-03-25 ImplSys,FT T-RpII,RTT-IB,FCIII,FbrLink |
00888867430358 - Arthrex® | 2024-03-25 ImplSys,FT T-RpII,RTT-IB,Drill,FbrLink |
00888867430365 - Arthrex® | 2024-03-25 ImplSys,FT T-RpII,RTT-IB,FLXDrill,FbrLin |
00888867462021 - Arthrex® | 2024-03-18 Dilator, 4.1 x 220mm |
00888867462038 - Arthrex® | 2024-03-18 Dilator, 5.1 x 210mm |
00888867462045 - Arthrex® | 2024-03-18 Dilator, 6.0 x 200mm |
00888867462052 - Arthrex® | 2024-03-18 Dilator, 7.1 x 190mm |
00888867462069 - Arthrex® | 2024-03-18 Dilator, 10.1 x 160mm |
Mark Image Registration | Serial | Company Trademark Application Date |
---|---|
SONOMA ORTHOPEDIC PRODUCTS, INC. 77903038 3898955 Live/Registered |
ARTHREX, INC. 2009-12-30 |