Kodiak
- Primary DI
- 00190376195827
- Brand
- Kodiak
- Company
- ALPHATEC SPINE, INC.
- Model
- 17031
- Device description
- Reduction Polyaxial Screwdriver, Power
- Published
- 2020-06-17
- Public version status
- New
- Distribution status
- In Commercial Distribution
- MRI safety
- Labeling does not contain MRI Safety Information
- Rx
- true
Contact Domains#
Product Codes#
| Code | Name |
|---|---|
| HWE | INSTRUMENT, SURGICAL, ORTHOPEDIC, AC-POWERED MOTOR AND ACCESSORY/ATTACHMENT |
Product Code Classifications#
| Code | Device | Specialty | Class |
|---|---|---|---|
| HWE | Instrument, Surgical, Orthopedic, Ac-Powered Motor And Accessory/Attachment | General, Plastic Surgery | 1 |
Identifiers And Packaging#
| Identifier | Type | Agency | Package quantity | Status |
|---|---|---|---|---|
| 00190376195827 | Primary | GS1 | 0 |
Alternate GTIN / UPC / EAN Codes
| Source identifier | GTIN-14 normalized | UPC-A | EAN-13 |
|---|---|---|---|
| 00190376195827 | 00190376195827 | 190376195827 | 0190376195827 |
GMDN Terms#
| Term | Definition |
|---|---|
| Surgical screwdriver, reusable | A non-powered tool intended to fit into a screw head (e.g., slotted, cross/hex head) for the application of rotation to introduce/remove a screw (e.g., craniofacial bone screw, dental screw) into/from a patient in association with a surgical procedure [e.g., orthopaedic, dental, computer assisted surgery (CAS), image registration]. It may also be used to connect/disconnect a device to/from another device attached to a patient (e.g., implant component, fiducial marker). The proximal end of the device may have a handle for manual use or a profiled tang that fits into an independent chuck or power driver; it is typically made of metallic and/or polymer materials. This is a reusable device. |
Sterilization Methods#
| Method |
|---|
| Moist Heat or Steam Sterilization |
Contacts#
| Phone | |
|---|---|
| +1(760)431-9286 | Regulatory@alphatecspine.com |
Regulatory Flags#
- DUNS number
- 602465783
- Device count
- 1
- Premarket exempt
- true
- Lot or batch
- true
- Sterilization required before use
- true
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|---|---|---|---|---|
| 00190376541471 | ATEC Lateral Navigation Disc Prep Instruments | 267-01-000-10-N | 2024-12-18 | |
| 00190376529158 | ATEC Posterior Navigation Disc Prep Instruments | 244-01-000-06-N | 2024-04-20 | |
| 00190376529189 | ATEC Posterior Navigation Disc Prep Instruments | 244-01-000-12-N | 2024-04-20 | |
| 00190376476162 | ATEC Lateral Navigation Disc Prep Instruments | 266-01-000-08-N | 2023-08-26 | |
| 00190376476179 | ATEC Lateral Navigation Disc Prep Instruments | 266-01-000-10-N | 2023-08-26 | |
| 00190376476186 | ATEC Lateral Navigation Disc Prep Instruments | 266-01-000-12-N | 2023-08-26 | |
| 00190376522906 | ATEC Lateral Navigation Disc Prep Instruments | 266-01-000-14-N | 2023-08-26 | |
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