Minit® 300-4018
GUDID 00889024333499
ZIMMER SPINE, INC.
Bone-screw internal spinal fixation system, non-sterile Bone-screw internal spinal fixation system, non-sterile Bone-screw internal spinal fixation system, non-sterile Bone-screw internal spinal fixation system, non-sterile Bone-screw internal spinal fixation system, non-sterile Bone-screw internal spinal fixation system, non-sterile Bone-screw internal spinal fixation system, non-sterile Bone-screw internal spinal fixation system, non-sterile Bone-screw internal spinal fixation system, non-sterile Bone-screw internal spinal fixation system, non-sterile Bone-screw internal spinal fixation system, non-sterile Bone-screw internal spinal fixation system, non-sterile Bone-screw internal spinal fixation system, non-sterile Bone-screw internal spinal fixation system, non-sterile Bone-screw internal spinal fixation system, non-sterile Bone-screw internal spinal fixation system, non-sterile Bone-screw internal spinal fixation system, non-sterile Bone-screw internal spinal fixation system, non-sterile Bone-screw internal spinal fixation system, non-sterile Bone-screw internal spinal fixation system, non-sterile Bone-screw internal spinal fixation system, non-sterile Bone-screw internal spinal fixation system, non-sterile Bone-screw internal spinal fixation system, non-sterile Bone-screw internal spinal fixation system, non-sterile Bone-screw internal spinal fixation system, non-sterile Bone-screw internal spinal fixation system, non-sterile Bone-screw internal spinal fixation system, non-sterile Bone-screw internal spinal fixation system, non-sterile Bone-screw internal spinal fixation system, non-sterile| Primary Device ID | 00889024333499 |
| NIH Device Record Key | 96925587-a5b5-4b9b-b0b2-e9d627d67b63 |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | Minit® |
| Version Model Number | 300-4018 |
| Catalog Number | 300-4018 |
| Company DUNS | 787663400 |
| Company Name | ZIMMER SPINE, 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 | 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
| Length | 18 Millimeter |
| Length | 18 Millimeter |
| Length | 18 Millimeter |
| Length | 18 Millimeter |
| Length | 18 Millimeter |
| Length | 18 Millimeter |
| Length | 18 Millimeter |
| Length | 18 Millimeter |
| Length | 18 Millimeter |
| Length | 18 Millimeter |
| Length | 18 Millimeter |
| Length | 18 Millimeter |
| Length | 18 Millimeter |
| Length | 18 Millimeter |
| Length | 18 Millimeter |
| Length | 18 Millimeter |
| Length | 18 Millimeter |
| Length | 18 Millimeter |
| Length | 18 Millimeter |
| Length | 18 Millimeter |
| Length | 18 Millimeter |
| Length | 18 Millimeter |
| Length | 18 Millimeter |
| Length | 18 Millimeter |
| Length | 18 Millimeter |
| Length | 18 Millimeter |
| Length | 18 Millimeter |
| Length | 18 Millimeter |
| Length | 18 Millimeter |
| Length | 18 Millimeter |
| Length | 18 Millimeter |
| Outer Diameter | 4 Millimeter |
| Length | 18 Millimeter |
| Outer Diameter | 4 Millimeter |
| Length | 18 Millimeter |
| Outer Diameter | 4 Millimeter |
| Length | 18 Millimeter |
| Outer Diameter | 4 Millimeter |
| Length | 18 Millimeter |
| Outer Diameter | 4 Millimeter |
| Length | 18 Millimeter |
| Outer Diameter | 4 Millimeter |
| Length | 18 Millimeter |
| Outer Diameter | 4 Millimeter |
| Length | 18 Millimeter |
| Outer Diameter | 4 Millimeter |
| Length | 18 Millimeter |
| Outer Diameter | 4 Millimeter |
| Length | 18 Millimeter |
| Outer Diameter | 4 Millimeter |
| Length | 18 Millimeter |
| Outer Diameter | 4 Millimeter |
| Length | 18 Millimeter |
| Outer Diameter | 4 Millimeter |
| Length | 18 Millimeter |
| Outer Diameter | 4 Millimeter |
| Length | 18 Millimeter |
Device Identifiers
| Device Issuing Agency | Device ID |
|---|---|
| GS1 | 00889024333499 [Primary] |
FDA Product Code
| KWP | APPLIANCE, FIXATION, SPINAL INTERLAMINAL |
Sterilization
| Steralize Prior To Use | true |
| Device Is Sterile | false |
[00889024333499]
Moist Heat or Steam Sterilization
[00889024333499]
Moist Heat or Steam Sterilization
[00889024333499]
Moist Heat or Steam Sterilization
[00889024333499]
Moist Heat or Steam Sterilization
[00889024333499]
Moist Heat or Steam Sterilization
[00889024333499]
Moist Heat or Steam Sterilization
[00889024333499]
Moist Heat or Steam Sterilization
[00889024333499]
Moist Heat or Steam Sterilization
[00889024333499]
Moist Heat or Steam Sterilization
[00889024333499]
Moist Heat or Steam Sterilization
[00889024333499]
Moist Heat or Steam Sterilization
[00889024333499]
Moist Heat or Steam Sterilization
[00889024333499]
Moist Heat or Steam Sterilization
[00889024333499]
Moist Heat or Steam Sterilization
[00889024333499]
Moist Heat or Steam Sterilization
[00889024333499]
Moist Heat or Steam Sterilization
[00889024333499]
Moist Heat or Steam Sterilization
[00889024333499]
Moist Heat or Steam Sterilization
[00889024333499]
Moist Heat or Steam Sterilization
[00889024333499]
Moist Heat or Steam Sterilization
[00889024333499]
Moist Heat or Steam Sterilization
[00889024333499]
Moist Heat or Steam Sterilization
[00889024333499]
Moist Heat or Steam Sterilization
[00889024333499]
Moist Heat or Steam Sterilization
[00889024333499]
Moist Heat or Steam Sterilization
[00889024333499]
Moist Heat or Steam Sterilization
[00889024333499]
Moist Heat or Steam Sterilization
[00889024333499]
Moist Heat or Steam Sterilization
[00889024333499]
Moist Heat or Steam Sterilization
Device Entry Metadata
| Public Version Status | Update |
| Device Record Status | Published |
| Public Version Number | 3 |
| Public Version Date | 2020-06-23 |
| Device Publish Date | 2015-09-24 |
On-Brand Devices [Minit®]
Trademark Results [Minit]
Mark Image Registration | Serial | Company Trademark Application Date |
|---|---|
 MINIT 97494942 not registered Live/Pending |
MLR INTERNATIONAL LLC 2022-07-08 |
 MINIT 86583370 4845848 Live/Registered |
MLR INTERNATIONAL LLC 2015-03-31 |
 MINIT 86321851 not registered Dead/Abandoned |
Whyte, Rodney T. 2014-06-26 |
 MINIT 86282656 4993870 Live/Registered |
Lead Technology Capital Management, LLC 2014-05-15 |
 MINIT 79248879 5809567 Live/Registered |
OXFORD NANOPORE TECHNOLOGIES LIMITED 2018-07-20 |
 MINIT 79167028 5178555 Live/Registered |
Minit j. s. a. 2015-03-27 |
 MINIT 78804390 3424386 Live/Registered |
Zimmer Biomet Spine, Inc. 2006-02-01 |
 MINIT 78532932 3028882 Dead/Cancelled |
MLR INTERNATIONAL LLC 2004-12-15 |
 MINIT 78429896 3235806 Dead/Cancelled |
SGB Group Limited 2004-06-04 |
 MINIT 77239540 3568270 Dead/Cancelled |
Weston Solutions (IPR), Inc. 2007-07-26 |
 MINIT 77239388 3544467 Dead/Cancelled |
Weston Solutions (IPR), Inc. 2007-07-26 |
 MINIT 75611738 2356998 Dead/Cancelled |
MERCHANDISING INTERNATIONAL S.A. 1998-12-23 |
© 2024 FDA.report
This site is not affiliated with or endorsed by the FDA.