TRITON
- Primary DI
- 00840996184472
- Brand
- TRITON
- Company
- Choice Spine, LP
- Model
- Q070-0009
- Device description
- TRITON,CANNULATED AWL
- Published
- 2023-07-06
- Public version status
- New
- Distribution status
- In Commercial Distribution
- MRI safety
- Labeling does not contain MRI Safety Information
- Rx
- true
- OTC
- false
- Sterile
- false
- Single use
- false
Related Records
Product Codes
| Code | Name |
|---|---|
| LXH | Orthopedic manual surgical instrument |
Product Code Classifications
| Code | Device | Specialty | Class |
|---|---|---|---|
| LXH | Orthopedic Manual Surgical Instrument | Orthopedic | 1 |
Premarket Submissions
| Submission | Supplement |
|---|---|
| K211449 | 000 |
Premarket Details
Identifiers And Packaging
| Identifier | Type | Agency | Package quantity | Status |
|---|---|---|---|---|
| 00840996184472 | Primary | GS1 | 0 |
Alternate GTIN / UPC / EAN Codes
| Source identifier | GTIN-14 normalized | UPC-A | EAN-13 |
|---|---|---|---|
| 00840996184472 | 00840996184472 | 840996184472 | 0840996184472 |
GMDN Terms
| Term | Definition |
|---|---|
| Sacroiliac joint transarticular fixation/arthrodesis implant, uncoated | An implantable device designed to be inserted across the sacroiliac joint to provide temporary stabilization and to encourage long-term joint fusion, typically to alleviate pain from the joint. It is made of uncoated metal [e.g., titanium (Ti)], and typically in the form of a cylinder which may be threaded and/or fenestrated. It is typically surgically implanted under fluoroscopic guidance and may include dedicated disposable implantation instruments. |
Sterilization Methods
| Method |
|---|
| Moist Heat or Steam Sterilization |
Regulatory Flags
- DUNS number
- 078293017
- Device count
- 1
- DM exempt
- true
- Premarket exempt
- false
- HCT/P
- false
- Kit
- false
- Combination product
- false
- Lot or batch
- true
- Serial number
- false
- Manufacturing date on label
- false
- Expiration date on label
- false
- Donation ID number
- false
- Contains natural rubber latex
- false
- No natural rubber latex
- false
- Sterilization required before use
- true
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|---|---|---|---|---|
| 00810211101256 | THUNDERBOLT | M070-0231 | 2026-02-13 | |
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| 00840996176569 | BOOMERANG | BT20-D4515 | 2026-01-15 | |
| 00840996176576 | Boomerang | BT20-D4517 | 2026-01-15 | |
| 00840996176583 | BOOMERANG | B070-0000 | 2026-01-15 | |
| 00840996176590 | BOOMERANG | B070-D010 | 2026-01-15 | |
| 00840996176606 | Boomerang | B070-0001 | 2026-01-15 | |
| 00840996182119 | HARRIER-SA Lumbar Interbody System | Y070-0043 | 2024-02-26 | |
| 00840996150682 | Acapella One | 05-099-05-1405 | 2024-02-24 | |
| 00840996150699 | Acapella One | 05-099-05-1406 | 2024-02-24 | |
| 00840996150705 | Acapella One | 05-099-05-1407 | 2024-02-24 | |
| 00840996150712 | Acapella One | 05-099-05-1408 | 2024-02-24 | |
| 00840996150729 | Acapella One | 05-099-05-1409 | 2024-02-24 | |
| 00840996150736 | Acapella One | 05-099-05-1410 | 2024-02-24 | |
| 00840996150743 | Acapella One | 05-099-05-1411 | 2024-02-24 | |
| 00840996150750 | Acapella One | 05-099-05-1412 | 2024-02-24 | |
| 00840996150767 | Acapella One | 05-099-05-1605 | 2024-02-24 | |
| 00840996150774 | Acapella One | 05-099-05-1606 | 2024-02-24 | |
| 00840996150781 | Acapella One | 05-099-05-1607 | 2024-02-24 | |
| 00840996150798 | Acapella One | 05-099-05-1608 | 2024-02-24 |
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