Sierra™
- Primary DI
- 10889910059042
- Brand
- Sierra™
- Company
- Seaspine Orthopedics Corporation
- Model
- 50-0135
- Catalog number
- 50-0135
- Device description
- Parallel Rod Connector, 3.5/3.5, Double. The Sierra occipito-cervico-thoracic (OCT) spinal fixation system, including polyaxial screws, rods, locking caps, occipital plates, occipital screws, lateral connectors, contoured crossbars, hooks, and components, is used to provide stabilization of the spine in order to permit the biological process of spinal fusion to occur. Accepted standard techniques of spinal fusion are an integral part of the implantation of this system.
- Published
- 2016-11-09
- Public version status
- Update
- Distribution status
- Not in Commercial Distribution
- MRI safety
- Labeling does not contain MRI Safety Information
- Rx
- true
Contact Domains#
Product Codes#
| Code | Name |
|---|---|
| KWP | APPLIANCE, FIXATION, SPINAL INTERLAMINAL |
Product Code Classifications#
| Code | Device | Specialty | Class |
|---|---|---|---|
| KWP | Appliance, Fixation, Spinal Interlaminal | Orthopedic | 2 |
Premarket Submissions#
| Submission | Supplement |
|---|---|
| K072729 | 000 |
Premarket Details#
Identifiers And Packaging#
| Identifier | Type | Agency | Package quantity | Status |
|---|---|---|---|---|
| 10889910059042 | Primary | GS1 | 0 |
Alternate GTIN / UPC / EAN Codes
| Source identifier | GTIN-14 normalized |
|---|---|
| 10889910059042 | 10889910059042 |
GMDN Terms#
| Term | Definition |
|---|---|
| Vertebral body prosthesis, non-sterile | A non-sterile implantable device designed to replace or repair (fuse) the spinal bony segments, or vertebrae, lost or injured as a consequence of, e.g., trauma, deformity, tumour, or degenerative disease. It is typically intended to be used with supplemental spinal fixation and may be used with a bone graft. It is usually made of metal, polymer, or a combination of these materials. This device must be sterilized prior to use. |
Device Sizes#
| Type | Value | Unit |
|---|---|---|
| Device Size Text, specify | 0 |
Sterilization Methods#
| Method |
|---|
| Moist Heat or Steam Sterilization |
Contacts#
| Phone | |
|---|---|
| +1(866)942-8698 | custsvcspine@seaspine.com |
Regulatory Flags#
- DUNS number
- 079840876
- Device count
- 1
- Lot or batch
- true
- Sterilization required before use
- true
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| 10889981172732 | Mariner Outrigger | 99-1012-12 | 99-1012-12 | 2019-07-30 |
| 10889981172749 | Mariner Outrigger | 99-1012-14 | 99-1012-14 | 2019-07-30 |
| 10889981172800 | Mariner Outrigger | 99-1015-14 | 99-1015-14 | 2019-07-30 |
| 10889981184940 | Mariner Outrigger | 99-1023-12 | 99-1023-12 | 2019-07-30 |
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| 10889981134945 | NewPort | 64-4755 | 64-4755 | 2024-12-11 |
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