Capstone Control Spinal System
- Primary DI
- 00643169674806
- Brand
- Capstone Control Spinal System
- Company
- MEDTRONIC SOFAMOR DANEK, INC.
- Model
- 4031527
- Device description
- SPACER 4031527 CONTROL 24 DEG 15X27
- Published
- 2023-10-02
- Public version status
- New
- Distribution status
- In Commercial Distribution
- MRI safety
- MR Conditional
- Sterile
- true
- Single use
- true
Contact Domains#
Product Codes#
| Code | Name |
|---|---|
| MAX | Intervertebral fusion device with bone graft, lumbar |
Product Code Classifications#
| Code | Device | Specialty | Class |
|---|---|---|---|
| MAX | Intervertebral Fusion Device With Bone Graft, Lumbar | Orthopedic | 2 |
Premarket Submissions#
| Submission | Supplement |
|---|---|
| K171107 | 000 |
Premarket Details#
Identifiers And Packaging#
| Identifier | Type | Agency | Package quantity | Status |
|---|---|---|---|---|
| 00643169674806 | Primary | GS1 | 0 |
Alternate GTIN / UPC / EAN Codes
| Source identifier | GTIN-14 normalized | UPC-A | EAN-13 |
|---|---|---|---|
| 00643169674806 | 00643169674806 | 643169674806 | 0643169674806 |
GMDN Terms#
| Term | Definition |
|---|---|
| Polymeric spinal interbody fusion cage | A device intended to be implanted into the space of an intervertebral disc that has been partially or totally removed during surgery in order to allow bone fusion between two contiguous vertebral bodies, typically in the treatment of degenerative disc disease (DDD). It is in the form of a hollow, porous, threaded and/or fenestrated cylindrical or geometrical device made of non-bioabsorbable synthetic polymer [e.g., polyetheretherketone (PEEK)] that provides mechanical stability and sufficient space for therapeutic spinal bone fusion to occur; bone graft is typically used to help with osseointegration. Fixation screws and devices associated with implantation may be included with the device. |
Device Sizes#
| Type | Value | Unit |
|---|---|---|
| Angle | 24 | degree |
| Height | 15 | Millimeter |
| Length | 27 | Millimeter |
Sterilization Methods#
| Method |
|---|
Contacts#
| Phone | |
|---|---|
| +1(800)633-8766 | Corporate.UDI@medtronic.com |
Regulatory Flags#
- DUNS number
- 830350380
- Device count
- 1
- Lot or batch
- true
- No natural rubber latex
- true
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| 00199150083879 | Medtronic Reusable Instruments | X0907411 | 2026-07-30 | |
| 00763000887216 | MSB CD HORIZON Spinal System | 6543535 | 2026-07-30 | |
| 00721902975158 | GDLH® Posterior Spinal System | X0196-111 | 2015-08-05 | |
| 00721902975189 | GDLH® Posterior Spinal System | X0196-122 | 2015-08-05 | |
| 00721902975219 | GDLH® Posterior Spinal System | X0196-126 | 2015-08-05 | |
| 00721902975226 | GDLH® Posterior Spinal System | X0196-128 | 2015-08-05 | |
| 00721902975233 | GDLH® Posterior Spinal System | X0196-130 | 2015-08-05 | |
| 00673978130316 | GDLH® Posterior Spinal System | X0196-104 | 2015-08-24 | |
| 00673978130347 | GDLH® Posterior Spinal System | X0196-107 | 2015-08-24 | |
| 00673978130361 | GDLH® Posterior Spinal System | X0196-109 | 2015-08-24 | |
| 00673978130385 | GDLH® Posterior Spinal System | X0196-112 | 2015-08-23 | |
| 00673978130392 | GDLH® Posterior Spinal System | X0196-114 | 2015-08-24 | |
| 00673978130408 | GDLH® Posterior Spinal System | X0196-116 | 2015-08-24 | |
| 00673978130415 | GDLH® Posterior Spinal System | X0196-118 | 2015-08-24 | |
| 00673978130422 | GDLH® Posterior Spinal System | X0196-120 | 2015-08-24 | |
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