Instinct™ Java® System
GUDID 00889024340251
ZIMMER SPINE
Bone-screw internal spinal fixation system, non-sterile| Primary Device ID | 00889024340251 |
| NIH Device Record Key | 73d9e39f-36be-4201-a92f-5bd9134efa92 |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | Instinct™ Java® System |
| Version Model Number | 046W0AN26530 |
| Company DUNS | 391738585 |
| Company Name | ZIMMER SPINE |
| 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 | false |
| Donation Id Number | false |
| Contains Natural Rubber Latex | false |
| Labeled No Natural Rubber Latex | false |
| RX Perscription | true |
| OTC Over-The-Counter | false |
Customer Support Contacts
Device Dimensions
| Device Size Text, specify | 0 |
| Length | 30 Millimeter |
| Device Size Text, specify | 0 |
| Length | 30 Millimeter |
| Device Size Text, specify | 0 |
| Length | 30 Millimeter |
| Device Size Text, specify | 0 |
| Length | 30 Millimeter |
| Device Size Text, specify | 0 |
| Length | 30 Millimeter |
| Device Size Text, specify | 0 |
| Length | 30 Millimeter |
| Device Size Text, specify | 0 |
| Length | 30 Millimeter |
| Device Size Text, specify | 0 |
| Length | 30 Millimeter |
| Device Size Text, specify | 0 |
| Length | 30 Millimeter |
| Device Size Text, specify | 0 |
| Length | 30 Millimeter |
| Device Size Text, specify | 0 |
| Length | 30 Millimeter |
| Device Size Text, specify | 0 |
| Length | 30 Millimeter |
| Device Size Text, specify | 0 |
| Length | 30 Millimeter |
| Device Size Text, specify | 0 |
| Length | 30 Millimeter |
| Device Size Text, specify | 0 |
| Length | 30 Millimeter |
| Device Size Text, specify | 0 |
| Length | 30 Millimeter |
| Device Size Text, specify | 0 |
| Length | 30 Millimeter |
| Device Size Text, specify | 0 |
| Length | 30 Millimeter |
| Device Size Text, specify | 0 |
| Length | 30 Millimeter |
| Device Size Text, specify | 0 |
| Length | 30 Millimeter |
| Device Size Text, specify | 0 |
| Length | 30 Millimeter |
| Device Size Text, specify | 0 |
| Length | 30 Millimeter |
| Device Size Text, specify | 0 |
| Length | 30 Millimeter |
| Device Size Text, specify | 0 |
| Length | 30 Millimeter |
| Device Size Text, specify | 0 |
| Length | 30 Millimeter |
| Device Size Text, specify | 0 |
Device Identifiers
| Device Issuing Agency | Device ID |
|---|---|
| GS1 | 00889024340251 [Primary] |
FDA Product Code
| MNH | Orthosis, spondylolisthesis spinal fixation |
Sterilization
| Steralize Prior To Use | true |
| Device Is Sterile | false |
[00889024340251]
Moist Heat or Steam Sterilization
[00889024340251]
Moist Heat or Steam Sterilization
[00889024340251]
Moist Heat or Steam Sterilization
[00889024340251]
Moist Heat or Steam Sterilization
[00889024340251]
Moist Heat or Steam Sterilization
[00889024340251]
Moist Heat or Steam Sterilization
[00889024340251]
Moist Heat or Steam Sterilization
[00889024340251]
Moist Heat or Steam Sterilization
[00889024340251]
Moist Heat or Steam Sterilization
[00889024340251]
Moist Heat or Steam Sterilization
[00889024340251]
Moist Heat or Steam Sterilization
[00889024340251]
Moist Heat or Steam Sterilization
[00889024340251]
Moist Heat or Steam Sterilization
[00889024340251]
Moist Heat or Steam Sterilization
[00889024340251]
Moist Heat or Steam Sterilization
[00889024340251]
Moist Heat or Steam Sterilization
[00889024340251]
Moist Heat or Steam Sterilization
[00889024340251]
Moist Heat or Steam Sterilization
[00889024340251]
Moist Heat or Steam Sterilization
[00889024340251]
Moist Heat or Steam Sterilization
[00889024340251]
Moist Heat or Steam Sterilization
[00889024340251]
Moist Heat or Steam Sterilization
[00889024340251]
Moist Heat or Steam Sterilization
[00889024340251]
Moist Heat or Steam Sterilization
[00889024340251]
Moist Heat or Steam Sterilization
[00889024340251]
Moist Heat or Steam Sterilization
Device Entry Metadata
| Public Version Status | Update |
| Device Record Status | Published |
| Public Version Number | 2 |
| Public Version Date | 2018-03-29 |
| Device Publish Date | 2015-10-02 |
On-Brand Devices [Instinct™ Java® System]
Trademark Results [Instinct]
Mark Image Registration | Serial | Company Trademark Application Date |
|---|---|
 INSTINCT 98730433 not registered Live/Pending |
MasterSpas, LLC 2024-09-03 |
 INSTINCT 98249219 not registered Live/Pending |
Robern, Inc. 2023-10-31 |
 INSTINCT 97398143 not registered Live/Pending |
Stylecraft, LLC 2022-05-06 |
 INSTINCT 90881910 not registered Live/Pending |
De la Puente, Juan E. 2021-08-13 |
 INSTINCT 90824913 not registered Live/Pending |
AHF, LLC 2021-07-13 |
 INSTINCT 90773170 not registered Live/Pending |
Jacobsen, Nefreteri K 2021-06-14 |
 INSTINCT 90751710 not registered Live/Pending |
Medtronic Minimed, Inc 2021-06-03 |
 INSTINCT 90597402 not registered Live/Pending |
ARC ABRASIVES, INC. 2021-03-23 |
 INSTINCT 90512837 not registered Live/Pending |
SA Consumer Products, Inc. 2021-02-05 |
 INSTINCT 88583503 not registered Live/Pending |
Raytheon Company 2019-08-19 |
 INSTINCT 88306387 5941987 Live/Registered |
Peaceful Pet Products LLC 2019-02-19 |
 INSTINCT 88226196 not registered Live/Pending |
Triangle Tube Phase III Co. 2018-12-12 |
© 2024 FDA.report
This site is not affiliated with or endorsed by the FDA.