Arristos
- Primary DI
- 00083672101565
- Brand
- Arristos
- Company
- INGENIUMSPINE, LLC
- Model
- 56000008
- Device description
- Rod Approximator
- Published
- 2018-10-10
- Public version status
- New
- Distribution status
- In Commercial Distribution
- MRI safety
- Labeling does n
- Rx
- true
- OTC
- false
- Sterile
- false
- Single use
- true
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 |
|---|---|
| K173126 | 000 |
Premarket Details#
Identifiers And Packaging#
| Identifier | Type | Agency | Package quantity | Status |
|---|---|---|---|---|
| 00083672101565 | Primary | GS1 | 0 |
Alternate GTIN / UPC / EAN Codes
| Source identifier | GTIN-14 normalized | UPC-A | EAN-13 |
|---|---|---|---|
| 00083672101565 | 00083672101565 | 083672101565 | 0083672101565 |
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 |
Regulatory Flags#
- DUNS number
- 082805471
- Device count
- 1
- DM exempt
- false
- 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
Other Devices From This Company#
| Primary DI | Brand | Model | Catalog | Published |
|---|---|---|---|---|
| 00843672101596 | Ingenix | 55027560 | 2022-05-14 | |
| 00843672101602 | Ingenix | 55026565 | 2022-05-14 | |
| 00843672101619 | Ingenix | 55027570 | 2022-05-14 | |
| 00843672101626 | Ingenix | 55027575 | 2022-05-14 | |
| 00843672101633 | Ingenix | 55027580 | 2022-05-14 | |
| 00843672101640 | Ingenix | 55017570 | 2022-05-14 | |
| 00843672101657 | Ingenix | 55017580 | 2022-05-14 | |
| 00843672100216 | INGENIX | 55016545 | 2018-06-15 | |
| 00843672100070 | INGENIX | 55015535 | 2018-06-15 | |
| 00843672100001 | INGENIX | 55014730 | 2018-06-15 | |
| 00843672100018 | INGENIX | 55014735 | 2018-06-15 | |
| 00843672100025 | INGENIX | 55014740 | 2018-06-15 | |
| 00843672100032 | INGENIX | 55014745 | 2018-06-15 | |
| 00843672100049 | INGENIX | 55014750 | 2018-06-15 | |
| 00843672100056 | INGENIX | 55014755 | 2018-06-15 | |
| 00843672100087 | INGENIX | 55015540 | 2018-06-15 | |
| 00843672100094 | INGENIX | 55015545 | 2018-06-15 | |
| 00843672100100 | INGENIX | 55015550 | 2018-06-15 | |
| 00843672100117 | INGENIX | 55015555 | 2018-06-15 | |
| 00843672100124 | INGENIX | 55016030 | 2018-06-15 |
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| 00763000992026 | MSB CD HORIZON Spinal System | MEDTRONIC SOFAMOR DANEK, INC. | KWP | 2026-08-02 |
| 00763000887216 | MSB CD HORIZON Spinal System | MEDTRONIC SOFAMOR DANEK, INC. | KWP | 2026-07-30 |
| 00840606189927 | OMEGA XP | SPINAL ELEMENTS, INC. | KWP | 2026-07-28 |
| 00841732168527 | TAURUS Pedicle Screw System | CTL Medical Corporation | KWP | 2026-07-28 |
| 10888857598164 | Xia® 3 System - Serrato® | VB Spine LLC | KWP | 2026-07-24 |
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