StruXure
- Primary DI
- 00887517411624
- Brand
- StruXure
- Company
- Nuvasive, Inc.
- Model
- 7006540
- Device description
- StruXure Screw, 6.5x40mm
- Published
- 2015-10-24
- Public version status
- Update
- Distribution status
- In Commercial Distribution
- MRI safety
- Labeling does not contain MRI Safety Information
- Rx
- true
Contact Domains#
Product Codes#
| Code | Name |
|---|---|
| KWQ | APPLIANCE, FIXATION, SPINAL INTERVERTEBRAL BODY |
Product Code Classifications#
| Code | Device | Specialty | Class |
|---|---|---|---|
| KWQ | Appliance, Fixation, Spinal Intervertebral Body | Orthopedic | 2 |
Premarket Submissions#
| Submission | Supplement |
|---|---|
| K111410 | 000 |
Premarket Details#
Identifiers And Packaging#
| Identifier | Type | Agency | Package quantity | Status |
|---|---|---|---|---|
| 00887517411624 | Primary | GS1 | 0 |
Alternate GTIN / UPC / EAN Codes
| Source identifier | GTIN-14 normalized | UPC-A | EAN-13 |
|---|---|---|---|
| 00887517411624 | 00887517411624 | 887517411624 | 0887517411624 |
GMDN Terms#
| Term | Definition |
|---|---|
| Bone-screw internal spinal fixation system, non-sterile | An assembly of non-sterile implantable devices intended to provide immobilization and stabilization of spinal segments in the treatment of various spinal instabilities or deformities, also used as an adjunct to spinal fusion [e.g., for degenerative disc disease (DDD)]. Otherwise known as a pedicle screw instrumentation system, it typically consists of a combination of anchors (e.g., bolts, hooks, pedicle screws or other types), interconnection mechanisms (incorporating nuts, screws, sleeves, or bolts), longitudinal members (e.g., plates, rods, plate/rod combinations), and/or transverse connectors. Non-sterile disposable devices associated with implantation may be included. |
Sterilization Methods#
| Method |
|---|
| Moist Heat or Steam Sterilization |
Contacts#
| Phone | |
|---|---|
| +1(858)909-1800 | RA_UDI@nuvasive.com |
| +1800-475-9131 | nuvainfo@globusmedical.com |
Regulatory Flags#
- DUNS number
- 053950783
- Device count
- 1
- Lot or batch
- true
- Sterilization required before use
- true
Other Devices From This Company#
| Primary DI | Brand | Model | Catalog | Published |
|---|---|---|---|---|
| 00887517614360 | Propel | 5020001 | 2015-09-24 | |
| 00887517614377 | Propel | 5020005 | 2015-09-24 | |
| 00887517614384 | Propel | 5020010 | 2015-09-24 | |
| 00887517939951 | AttraX | 5015110 | 2018-06-05 | |
| 00887517939968 | AttraX | 5015120 | 2018-06-05 | |
| 00887517939975 | AttraX | 5015130 | 2018-06-05 | |
| 00887517939982 | AttraX | 5015103 | 2018-06-05 | |
| 00887517939999 | AttraX | 5015104 | 2018-06-05 | |
| 00887517940001 | AttraX | 5015106 | 2018-06-05 | |
| 00887517940018 | AttraX | 5015101 | 2018-06-05 | |
| 00887517940025 | AttraX | 5015102 | 2018-06-05 | |
| 00887517970435 | Propel | 5020205 | 2018-12-20 | |
| 00887517970442 | Propel | 5020205994 | 2018-12-20 | |
| 00887517970459 | Propel | 5020210 | 2018-12-20 | |
| 00887517970466 | Propel | 5020210994 | 2018-12-20 | |
| 00887517970473 | Propel | 5020301 | 2018-12-20 | |
| 00887517970480 | Propel | 5020301994 | 2018-12-20 | |
| 00887517970497 | Propel | 5020305 | 2018-12-20 | |
| 00887517971500 | Propel | 5020305994 | 2018-12-20 | |
| 00887517971517 | Propel | 5020310 | 2018-12-20 |
Other Devices Sharing Product Codes#
| Primary DI | Brand | Company | Product code | Published |
|---|---|---|---|---|
| 00763000786458 | CD HORIZONĀ® Fenestrated Screw Spinal System | MEDTRONIC SOFAMOR DANEK, INC. | KWQ | 2026-10-15 |
| 10889981217204 | Meridian | Seaspine Orthopedics Corporation | KWQ | 2022-08-25 |
| 10889981230838 | Regatta | Seaspine Orthopedics Corporation | KWQ | 2021-02-02 |
| 10889981230845 | Regatta | Seaspine Orthopedics Corporation | KWQ | 2021-02-02 |
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