UCSS® Screw Set
GUDID 00721902319655
4.0 CORTICAL BONE SCREW 40MM
MEDTRONIC SOFAMOR DANEK, INC.
Bone-screw internal spinal fixation system, non-sterile| Primary Device ID | 00721902319655 |
| NIH Device Record Key | 41cf2eb9-f578-4054-830c-3e88c86909fc |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | UCSS® Screw Set |
| Version Model Number | 9098540 |
| Company DUNS | 830350380 |
| Company Name | MEDTRONIC SOFAMOR DANEK, 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 | 40 Millimeter |
| Length | 40 Millimeter |
| Length | 40 Millimeter |
| Length | 40 Millimeter |
| Outer Diameter | 4 Millimeter |
| Length | 40 Millimeter |
| Outer Diameter | 4 Millimeter |
| Length | 40 Millimeter |
| Outer Diameter | 4 Millimeter |
| Length | 40 Millimeter |
| Outer Diameter | 4 Millimeter |
| Length | 40 Millimeter |
| Outer Diameter | 4 Millimeter |
| Length | 40 Millimeter |
| Outer Diameter | 4 Millimeter |
| Length | 40 Millimeter |
| Outer Diameter | 4 Millimeter |
| Length | 40 Millimeter |
| Outer Diameter | 4 Millimeter |
| Length | 40 Millimeter |
| Outer Diameter | 4 Millimeter |
| Length | 40 Millimeter |
| Outer Diameter | 4 Millimeter |
| Length | 40 Millimeter |
| Outer Diameter | 4 Millimeter |
| Length | 40 Millimeter |
| Outer Diameter | 4 Millimeter |
| Length | 40 Millimeter |
| Outer Diameter | 4 Millimeter |
| Length | 40 Millimeter |
| Outer Diameter | 4 Millimeter |
| Length | 40 Millimeter |
| Outer Diameter | 4 Millimeter |
| Length | 40 Millimeter |
| Outer Diameter | 4 Millimeter |
| Length | 40 Millimeter |
| Outer Diameter | 4 Millimeter |
| Length | 40 Millimeter |
| Outer Diameter | 4 Millimeter |
| Length | 40 Millimeter |
| Outer Diameter | 4 Millimeter |
| Length | 40 Millimeter |
| Outer Diameter | 4 Millimeter |
| Length | 40 Millimeter |
| Outer Diameter | 4 Millimeter |
| Length | 40 Millimeter |
| Outer Diameter | 4 Millimeter |
| Length | 40 Millimeter |
| Outer Diameter | 4 Millimeter |
| Length | 40 Millimeter |
| Outer Diameter | 4 Millimeter |
| Length | 40 Millimeter |
| Outer Diameter | 4 Millimeter |
| Length | 40 Millimeter |
| Outer Diameter | 4 Millimeter |
| Length | 40 Millimeter |
| Outer Diameter | 4 Millimeter |
| Length | 40 Millimeter |
| Outer Diameter | 4 Millimeter |
| Length | 40 Millimeter |
Device Identifiers
| Device Issuing Agency | Device ID |
|---|---|
| GS1 | 00721902319655 [Primary] |
FDA Pre-market Approvals/Notifications & deNovo
- Premarket Notification: K013829
FDA Product Code
| MRW | SYSTEM, FACET SCREW SPINAL DEVICE |
Sterilization
| Steralize Prior To Use | true |
| Device Is Sterile | false |
[00721902319655]
Moist Heat or Steam Sterilization
[00721902319655]
Moist Heat or Steam Sterilization
[00721902319655]
Moist Heat or Steam Sterilization
[00721902319655]
Moist Heat or Steam Sterilization
[00721902319655]
Moist Heat or Steam Sterilization
[00721902319655]
Moist Heat or Steam Sterilization
[00721902319655]
Moist Heat or Steam Sterilization
[00721902319655]
Moist Heat or Steam Sterilization
[00721902319655]
Moist Heat or Steam Sterilization
[00721902319655]
Moist Heat or Steam Sterilization
[00721902319655]
Moist Heat or Steam Sterilization
[00721902319655]
Moist Heat or Steam Sterilization
[00721902319655]
Moist Heat or Steam Sterilization
[00721902319655]
Moist Heat or Steam Sterilization
[00721902319655]
Moist Heat or Steam Sterilization
[00721902319655]
Moist Heat or Steam Sterilization
[00721902319655]
Moist Heat or Steam Sterilization
[00721902319655]
Moist Heat or Steam Sterilization
[00721902319655]
Moist Heat or Steam Sterilization
[00721902319655]
Moist Heat or Steam Sterilization
[00721902319655]
Moist Heat or Steam Sterilization
[00721902319655]
Moist Heat or Steam Sterilization
[00721902319655]
Moist Heat or Steam Sterilization
[00721902319655]
Moist Heat or Steam Sterilization
[00721902319655]
Moist Heat or Steam Sterilization
[00721902319655]
Moist Heat or Steam Sterilization
[00721902319655]
Moist Heat or Steam Sterilization
[00721902319655]
Moist Heat or Steam Sterilization
[00721902319655]
Moist Heat or Steam Sterilization
[00721902319655]
Moist Heat or Steam Sterilization
Device Entry Metadata
| Public Version Status | Update |
| Device Record Status | Published |
| Public Version Number | 3 |
| Public Version Date | 2018-07-06 |
| Device Publish Date | 2015-07-30 |
On-Brand Devices [UCSS® Screw Set]
| 00613994264237 | SCREW X10043510 TI 3.5X10MM THRPST |
| 00673978067971 | BONE SCREW 873-150 4.0 CAN CORT LAG L 50 |
| 00673978067964 | BONE SCREW 873-148 4.0 CAN CORT LAG L 48 |
| 00673978067957 | BONE SCREW 873-146 4.0 CAN CORT LAG L 46 |
| 00673978067940 | BONE SCREW 873-144 4.0 CAN CORT LAG L 44 |
| 00673978067933 | BONE SCREW 873-142 4.0 CAN CORT LAG L 42 |
| 00673978067926 | BONE SCREW 873-140 4.0 CAN CORT LAG L 40 |
| 00673978067919 | BONE SCREW 873-138 4.0 CAN CORT LAG L 38 |
| 00673978067902 | BONE SCREW 873-136 4.0 CAN CORT LAG L 36 |
| 00673978067896 | BONE SCREW 873-050 4.0 CANN CORT L 50MM |
| 00673978067889 | BONE SCREW 873-048 4.0 CANN CORT L 48MM |
| 00673978067872 | BONE SCREW 873-046 4.0 CANN CORT L 46MM |
| 00673978067865 | BONE SCREW 873-044 4.0 CANN CORT L 44MM |
| 00673978067858 | BONE SCREW 873-042 4.0 CANN CORT L 42MM |
| 00673978067841 | BONE SCREW 873-040 4.0 CANN CORT L 40MM |
| 00673978067834 | BONE SCREW 873-038 4.0 CANN CORT L 38MM |
| 00673978067827 | BONE SCREW 873-036 4.0 CANN CORT L 36MM |
| 00673978067810 | BONE SCREW 873-034 4.0 CANN CORT L 34MM |
| 00673978067803 | BONE SCREW 873-032 4.0 CANN CORT L 32MM |
| 00673978067797 | BONE SCREW 873-030 4.0 CANN CORT L 30MM |
| 00721902613371 | UCS DBLTHDSCR-TI-CANN-4.0X40 |
| 00721902319815 | 4.0 CORTICAL BONE SCREW 60MM |
| 00721902319792 | 4.0 CORTICAL BONE SCREW 58MM |
| 00721902319785 | 4.0 CORTICAL BONE SCREW 56MM |
| 00721902319778 | 4.0 CORTICAL BONE SCREW 54MM |
| 00721902319747 | 4.0 CORTICAL BONE SCREW 52MM |
| 00721902319730 | 4.0 CORTICAL BONE SCREW 50MM |
| 00721902319709 | 4.0 CORTICAL BONE SCREW 48MM |
| 00721902319693 | 4.0 CORTICAL BONE SCREW 46MM |
| 00721902319686 | 4.0 CORTICAL BONE SCREW 44MM |
| 00721902319679 | 4.0 CORTICAL BONE SCREW 42MM |
| 00721902319655 | 4.0 CORTICAL BONE SCREW 40MM |
| 00721902319617 | 4.0 CORTICAL BONE SCREW 38MM |
| 00721902319532 | 4.0 CORTICAL BONE SCREW 34MM |
| 00721902319518 | 4.0 CORTICAL BONE SCREW 30MM |
| 00721902319495 | 4.0 CORTICAL BONE SCREW 26MM |
| 00673978067759 | CASE 873-012 UCSS INSTRUMENT MODULE |
Trademark Results [UCSS]
Mark Image Registration | Serial | Company Trademark Application Date |
|---|---|
 UCSS 78357555 2974437 Live/Registered |
WARSAW ORTHOPEDIC, INC. 2004-01-26 |
 UCSS 75557936 not registered Dead/Abandoned |
SDGI Holdings, Inc. 1998-09-23 |
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