TECHTONIX 48204658
GUDID 07613154108114
46-58 mm PLATE LONG
Stryker Corporation
Bone-screw internal spinal fixation system, non-sterile Spinal fixation plate, non-bioabsorbable Spinal fixation plate, non-bioabsorbable Spinal fixation plate, non-bioabsorbable Spinal fixation plate, non-bioabsorbable Spinal fixation plate, non-bioabsorbable Spinal fixation plate, non-bioabsorbable Spinal fixation plate, non-bioabsorbable Spinal fixation plate, non-bioabsorbable Spinal fixation plate, non-bioabsorbable Spinal fixation plate, non-bioabsorbable Spinal fixation plate, non-bioabsorbable Spinal fixation plate, non-bioabsorbable Spinal fixation plate, non-bioabsorbable Spinal fixation plate, non-bioabsorbable Spinal fixation plate, non-bioabsorbable Spinal fixation plate, non-bioabsorbable Spinal fixation plate, non-bioabsorbable Spinal fixation plate, non-bioabsorbable Spinal fixation plate, non-bioabsorbable Spinal fixation plate, non-bioabsorbable Spinal fixation plate, non-bioabsorbable Spinal fixation plate, non-bioabsorbable Spinal fixation plate, non-bioabsorbable Spinal fixation plate, non-bioabsorbable Spinal fixation plate, non-bioabsorbable Spinal fixation plate, non-bioabsorbable Spinal fixation plate, non-bioabsorbable Spinal fixation plate, non-bioabsorbable Spinal fixation plate, non-bioabsorbable Spinal fixation plate, non-bioabsorbable Spinal fixation plate, non-bioabsorbable| Primary Device ID | 07613154108114 |
| NIH Device Record Key | d9d9a5bd-2e97-4a8d-8de3-904b5d90d375 |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | TECHTONIX |
| Version Model Number | 48204658 |
| Catalog Number | 48204658 |
| Company DUNS | 149183167 |
| Company Name | Stryker Corporation |
| 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 | false |
| Donation Id Number | false |
| Contains Natural Rubber Latex | false |
| Labeled No Natural Rubber Latex | false |
| RX Perscription | true |
| OTC Over-The-Counter | false |
Device Identifiers
| Device Issuing Agency | Device ID |
|---|---|
| GS1 | 07613154108114 [Primary] |
FDA Product Code
| KWP | APPLIANCE, FIXATION, SPINAL INTERLAMINAL |
Sterilization
| Steralize Prior To Use | true |
| Device Is Sterile | false |
[07613154108114]
Moist Heat or Steam Sterilization
[07613154108114]
Moist Heat or Steam Sterilization
[07613154108114]
Moist Heat or Steam Sterilization
[07613154108114]
Moist Heat or Steam Sterilization
[07613154108114]
Moist Heat or Steam Sterilization
[07613154108114]
Moist Heat or Steam Sterilization
[07613154108114]
Moist Heat or Steam Sterilization
[07613154108114]
Moist Heat or Steam Sterilization
[07613154108114]
Moist Heat or Steam Sterilization
[07613154108114]
Moist Heat or Steam Sterilization
[07613154108114]
Moist Heat or Steam Sterilization
[07613154108114]
Moist Heat or Steam Sterilization
[07613154108114]
Moist Heat or Steam Sterilization
[07613154108114]
Moist Heat or Steam Sterilization
[07613154108114]
Moist Heat or Steam Sterilization
[07613154108114]
Moist Heat or Steam Sterilization
[07613154108114]
Moist Heat or Steam Sterilization
[07613154108114]
Moist Heat or Steam Sterilization
[07613154108114]
Moist Heat or Steam Sterilization
[07613154108114]
Moist Heat or Steam Sterilization
[07613154108114]
Moist Heat or Steam Sterilization
[07613154108114]
Moist Heat or Steam Sterilization
[07613154108114]
Moist Heat or Steam Sterilization
[07613154108114]
Moist Heat or Steam Sterilization
[07613154108114]
Moist Heat or Steam Sterilization
[07613154108114]
Moist Heat or Steam Sterilization
[07613154108114]
Moist Heat or Steam Sterilization
[07613154108114]
Moist Heat or Steam Sterilization
[07613154108114]
Moist Heat or Steam Sterilization
[07613154108114]
Moist Heat or Steam Sterilization
[07613154108114]
Moist Heat or Steam Sterilization
[07613154108114]
Moist Heat or Steam Sterilization
Device Entry Metadata
| Public Version Status | Update |
| Device Record Status | Published |
| Public Version Number | 4 |
| Public Version Date | 2018-11-26 |
| Device Publish Date | 2015-09-14 |
On-Brand Devices [TECHTONIX]
| 07613327066708 | SCREW |
| 07613327066692 | SCREW |
| 07613327066685 | SCREW |
| 07613154108893 | SCREW |
| 07613154108824 | SCREW |
| 07613154108817 | SCREW |
| 07613154108114 | 46-58 mm PLATE LONG |
| 04546540496478 | 4.5 mm BLOCKER |
| 04546540443816 | SCREW |
| 04546540443809 | SCREW |
| 04546540443793 | SCREW |
| 04546540443786 | SCREW |
| 04546540443779 | SCREW |
| 04546540443731 | SCREW |
| 04546540443724 | SCREW |
| 04546540443717 | SCREW |
| 04546540443700 | SCREW |
| 04546540443694 | SCREW |
| 04546540443151 | 28-40 mm PLATE MEDIUM LONG |
| 04546540443144 | 22-34 mm PLATE SHORT MEDIUM |
| 04546540443137 | PLATE SHORT |
| 07613327264791 | GEARSHIFT PROBE STRAIGHT |
| 07613327264821 | TORQUE WRENCH SOCKET |
| 07613327264784 | DISTRACTOR |
Trademark Results [TECHTONIX]
Mark Image Registration | Serial | Company Trademark Application Date |
|---|---|
 TECHTONIX 85832763 4512155 Live/Registered |
TECHTONIX, INC. 2013-01-25 |
 TECHTONIX 78489998 3121853 Live/Registered |
STRYKER EUROPEAN HOLDINGS I, LLC 2004-09-27 |
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