THOR 480316052
GUDID 07613327065480
STANDARD SCREW
Stryker Corporation
Spinal fixation plate, non-bioabsorbable| Primary Device ID | 07613327065480 |
| NIH Device Record Key | 7612b2e0-ec64-4182-952b-b0bf849bfeaf |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | THOR |
| Version Model Number | 480316052 |
| Catalog Number | 480316052 |
| 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 Dimensions
| Length | 52 Millimeter |
| Device Size Text, specify | 0 |
| Length | 52 Millimeter |
| Device Size Text, specify | 0 |
| Length | 52 Millimeter |
| Device Size Text, specify | 0 |
| Length | 52 Millimeter |
| Device Size Text, specify | 0 |
| Length | 52 Millimeter |
| Device Size Text, specify | 0 |
| Length | 52 Millimeter |
| Device Size Text, specify | 0 |
| Length | 52 Millimeter |
| Device Size Text, specify | 0 |
| Length | 52 Millimeter |
| Device Size Text, specify | 0 |
| Length | 52 Millimeter |
| Device Size Text, specify | 0 |
| Length | 52 Millimeter |
| Device Size Text, specify | 0 |
| Length | 52 Millimeter |
| Device Size Text, specify | 0 |
| Length | 52 Millimeter |
| Device Size Text, specify | 0 |
| Length | 52 Millimeter |
| Device Size Text, specify | 0 |
| Length | 52 Millimeter |
| Device Size Text, specify | 0 |
| Length | 52 Millimeter |
| Device Size Text, specify | 0 |
| Length | 52 Millimeter |
| Device Size Text, specify | 0 |
| Length | 52 Millimeter |
| Device Size Text, specify | 0 |
| Length | 52 Millimeter |
| Device Size Text, specify | 0 |
| Length | 52 Millimeter |
| Device Size Text, specify | 0 |
| Length | 52 Millimeter |
| Device Size Text, specify | 0 |
| Length | 52 Millimeter |
| Device Size Text, specify | 0 |
| Length | 52 Millimeter |
| Device Size Text, specify | 0 |
| Length | 52 Millimeter |
| Device Size Text, specify | 0 |
| Length | 52 Millimeter |
| Device Size Text, specify | 0 |
| Length | 52 Millimeter |
| Device Size Text, specify | 0 |
| Length | 52 Millimeter |
| Device Size Text, specify | 0 |
| Length | 52 Millimeter |
| Device Size Text, specify | 0 |
| Length | 52 Millimeter |
| Device Size Text, specify | 0 |
| Length | 52 Millimeter |
| Device Size Text, specify | 0 |
| Length | 52 Millimeter |
| Device Size Text, specify | 0 |
Device Identifiers
| Device Issuing Agency | Device ID |
|---|---|
| GS1 | 07613327065480 [Primary] |
FDA Product Code
| KWQ | APPLIANCE, FIXATION, SPINAL INTERVERTEBRAL BODY |
Sterilization
| Steralize Prior To Use | true |
| Device Is Sterile | false |
[07613327065480]
Moist Heat or Steam Sterilization
[07613327065480]
Moist Heat or Steam Sterilization
[07613327065480]
Moist Heat or Steam Sterilization
[07613327065480]
Moist Heat or Steam Sterilization
[07613327065480]
Moist Heat or Steam Sterilization
[07613327065480]
Moist Heat or Steam Sterilization
[07613327065480]
Moist Heat or Steam Sterilization
[07613327065480]
Moist Heat or Steam Sterilization
[07613327065480]
Moist Heat or Steam Sterilization
[07613327065480]
Moist Heat or Steam Sterilization
[07613327065480]
Moist Heat or Steam Sterilization
[07613327065480]
Moist Heat or Steam Sterilization
[07613327065480]
Moist Heat or Steam Sterilization
[07613327065480]
Moist Heat or Steam Sterilization
[07613327065480]
Moist Heat or Steam Sterilization
[07613327065480]
Moist Heat or Steam Sterilization
[07613327065480]
Moist Heat or Steam Sterilization
[07613327065480]
Moist Heat or Steam Sterilization
[07613327065480]
Moist Heat or Steam Sterilization
[07613327065480]
Moist Heat or Steam Sterilization
[07613327065480]
Moist Heat or Steam Sterilization
[07613327065480]
Moist Heat or Steam Sterilization
[07613327065480]
Moist Heat or Steam Sterilization
[07613327065480]
Moist Heat or Steam Sterilization
[07613327065480]
Moist Heat or Steam Sterilization
[07613327065480]
Moist Heat or Steam Sterilization
[07613327065480]
Moist Heat or Steam Sterilization
[07613327065480]
Moist Heat or Steam Sterilization
[07613327065480]
Moist Heat or Steam Sterilization
[07613327065480]
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 | 2015-09-14 |
On-Brand Devices [THOR]
| 07613327067477 | COMPRESSION SCREW |
| 07613327067460 | COMPRESSION SCREW |
| 07613327067453 | THORACOLUMBAR PLATE |
| 07613327067446 | THORACOLUMBAR PLATE |
| 07613327067439 | THORACOLUMBAR PLATE |
| 07613327067422 | THORACOLUMBAR PLATE |
| 07613327067415 | THORACOLUMBAR PLATE |
| 07613327067408 | THORACOLUMBAR PLATE |
| 07613327067392 | THORACOLUMBAR PLATE |
| 07613327067385 | THORACOLUMBAR PLATE |
| 07613327067378 | THORACOLUMBAR PLATE |
| 07613327067361 | THORACOLUMBAR PLATE |
| 07613327067354 | THORACOLUMBAR PLATE |
| 07613327067347 | THORACOLUMBAR PLATE |
| 07613327067330 | THORACOLUMBAR PLATE |
| 07613327067323 | THORACOLUMBAR PLATE |
| 07613327067316 | THORACOLUMBAR PLATE |
| 07613327067309 | THORACOLUMBAR PLATE |
| 07613327067293 | STANDARD SCREW |
| 07613327067286 | STANDARD SCREW |
| 07613327067279 | STANDARD SCREW |
| 07613327067262 | STANDARD SCREW |
| 07613327067255 | STANDARD SCREW |
| 07613327067248 | STANDARD SCREW |
| 07613327067231 | STANDARD SCREW |
| 07613327067224 | STANDARD SCREW |
| 07613327067217 | STANDARD SCREW |
| 07613327067200 | STANDARD SCREW |
| 07613327067194 | STANDARD SCREW |
| 07613327067187 | STANDARD SCREW |
| 07613327067170 | STANDARD SCREW |
| 07613327067163 | STANDARD SCREW |
| 07613327067156 | STANDARD SCREW |
| 07613327067149 | STANDARD SCREW |
| 07613327067132 | STANDARD SCREW |
| 07613327067125 | STANDARD SCREW |
| 07613327065480 | STANDARD SCREW |
| 07613327065435 | STANDARD SCREW |
| 07613327065428 | STANDARD SCREW |
| 07613327065411 | STANDARD SCREW |
| 07613327065404 | STANDARD SCREW |
| 07613327065398 | STANDARD SCREW |
| 07613327065381 | STANDARD SCREW |
| 07613327065374 | STANDARD SCREW |
| 07613327065367 | STANDARD SCREW |
| 07613327065350 | STANDARD SCREW |
| 07613327065343 | STANDARD SCREW |
| 07613327065336 | COMPRESSION SCREW |
| 07613327065329 | TWO LEVEL SACRAL COMPRESSION PLATE |
| 07613327065312 | TWO LEVEL SACRAL COMPRESSION PLATE |
Trademark Results [THOR]
Mark Image Registration | Serial | Company Trademark Application Date |
|---|---|
 THOR 98460872 not registered Live/Pending |
Milton Industries, Inc. 2024-03-21 |
 THOR 98035719 not registered Live/Pending |
PETROMAC IP LIMITED 2023-06-09 |
 THOR 97741551 not registered Live/Pending |
HONGKONG DINGXIN INDUSTRY AND TRADE LIMITED 2023-01-04 |
 THOR 97741548 not registered Live/Pending |
HONGKONG DINGXIN INDUSTRY AND TRADE LIMITED 2023-01-04 |
 THOR 97660133 not registered Live/Pending |
Allness Brands 2022-11-02 |
 THOR 97608705 not registered Live/Pending |
AUSA Premium Cigar Holdings Inc. 2022-09-27 |
 THOR 97589814 not registered Live/Pending |
RooSportz LLC 2022-09-13 |
 THOR 97494656 not registered Live/Pending |
EnQuest Energy Solutions LLC 2022-07-08 |
 THOR 97494653 not registered Live/Pending |
EnQuest Energy Solutions LLC 2022-07-08 |
 THOR 97458252 not registered Live/Pending |
Yo Corp. 2022-06-14 |
 THOR 97303357 not registered Live/Pending |
Thor Miner Inc. 2022-03-09 |
 THOR 97117481 not registered Live/Pending |
Yo Corp. 2021-11-10 |
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