PRECICE® UNYTE Trauma Nail System T12.5-80A275
GUDID 00887517937483
Trauma Retro Femur 10°, 12.5x275mm
NUVASIVE SPECIALIZED ORTHOPEDICS, INC.
Long bone distraction rod, magnetic Long bone distraction rod, magnetic Long bone distraction rod, magnetic Long bone distraction rod, magnetic Long bone distraction rod, magnetic Long bone distraction rod, magnetic Long bone distraction rod, magnetic Long bone distraction rod, magnetic Long bone distraction rod, magnetic Long bone distraction rod, magnetic Long bone distraction rod, magnetic Long bone distraction rod, magnetic Long bone distraction rod, magnetic Long bone distraction rod, magnetic Long bone distraction rod, magnetic Long bone distraction rod, magnetic Long bone distraction nail, magnetic Long bone distraction nail, magnetic Long bone distraction nail, magnetic Long bone distraction nail, magnetic Long bone distraction nail, magnetic Long bone distraction nail, magnetic Long bone distraction nail, magnetic Long bone distraction nail, magnetic Long bone distraction nail, magnetic Long bone distraction nail, magnetic Long bone distraction nail, magnetic Long bone distraction nail, magnetic Long bone distraction nail, magnetic| Primary Device ID | 00887517937483 |
| NIH Device Record Key | 838593e8-4f91-4f4e-97d6-bff8d4741590 |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | PRECICE® UNYTE Trauma Nail System |
| Version Model Number | T12.5-80A275 |
| Catalog Number | T12.5-80A275 |
| Company DUNS | 837845234 |
| Company Name | NUVASIVE SPECIALIZED ORTHOPEDICS, INC. |
| Device Count | 1 |
| DM Exempt | false |
| Pre-market Exempt | false |
| MRI Safety Status | MR Unsafe |
| 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 | true |
| 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 Identifiers
| Device Issuing Agency | Device ID |
|---|---|
| GS1 | 00887517937483 [Primary] |
FDA Product Code
| HSB | Rod, Fixation, Intramedullary And Accessories |
Sterilization
| Steralize Prior To Use | false |
| Device Is Sterile | true |
Device Entry Metadata
| Public Version Status | New |
| Device Record Status | Published |
| Public Version Number | 1 |
| Public Version Date | 2021-02-23 |
| Device Publish Date | 2021-02-15 |
On-Brand Devices [PRECICE® UNYTE Trauma Nail System]
| 00887517937506 | Trauma Retro Femur 10°, 12.5x335mm |
| 00887517937490 | Trauma Retro Femur 10°, 12.5x305mm |
| 00887517937483 | Trauma Retro Femur 10°, 12.5x275mm |
| 00887517937476 | Trauma Retro Femur 10°, 10.7x335mm |
| 00887517937469 | Trauma Retro Femur 10°, 10.7x305mm |
| 00887517937452 | Trauma Retro Femur 10°, 10.7x275mm |
Trademark Results [PRECICE]
Mark Image Registration | Serial | Company Trademark Application Date |
|---|---|
 PRECICE 97287304 not registered Live/Pending |
PRECICE MOTORSPORTS LLC 2022-02-28 |
 PRECICE 88073801 not registered Live/Pending |
Epic Ice, LLC 2018-08-10 |
 PRECICE 85064864 4158334 Live/Registered |
NUVASIVE, INC. 2010-06-16 |
 PRECICE 76250632 not registered Dead/Abandoned |
KLA-Tencor Corporation 2001-05-03 |
 PRECICE 75092861 not registered Dead/Abandoned |
Cadence Design Systems, Inc. 1996-04-23 |
 PRECICE 75072688 not registered Dead/Abandoned |
BIODEX MEDICAL SYSTEMS, INC. 1996-03-14 |
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