Navigated Anterolateral Disc Prep Instruments
- Primary DI
- 00763000200848
- Brand
- Navigated Anterolateral Disc Prep Instruments
- Company
- MEDTRONIC SOFAMOR DANEK, INC.
- Model
- NAV4680011
- Device description
- CURETTE NAV4680011 NAV 45 DEG PULL 5MM
- Published
- 2020-02-12
- 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 |
|---|---|
| OLO | Orthopedic stereotaxic instrument |
Product Code Classifications#
| Code | Device | Specialty | Class |
|---|---|---|---|
| OLO | Orthopedic Stereotaxic Instrument | Neurology | 2 |
Premarket Submissions#
| Submission | Supplement |
|---|---|
| K192336 | 000 |
Premarket Details#
Identifiers And Packaging#
| Identifier | Type | Agency | Package quantity | Status |
|---|---|---|---|---|
| 00763000200848 | Primary | GS1 | 0 |
Alternate GTIN / UPC / EAN Codes
| Source identifier | GTIN-14 normalized | UPC-A | EAN-13 |
|---|---|---|---|
| 00763000200848 | 00763000200848 | 763000200848 | 0763000200848 |
GMDN Terms#
| Term | Definition |
|---|---|
| Bone curette, reusable | A manual surgical instrument designed for cutting and excising bone tissue typically during an orthopaedic or a plastic surgery procedure. It is typically designed as a long, slender instrument with a handle at the proximal end and a concave, spoon-like tip which has a sharp edge, at the distal end, or it may be double-ended, and is used to facilitate the removal of the bone tissue without causing trauma to the surrounding muscles. It is typically made of high-grade stainless steel and is a common instrument of choice for the removal of the bone. This is a reusable device. |
Device Sizes#
| Type | Value | Unit |
|---|---|---|
| Length | 5.5 | Millimeter |
Sterilization Methods#
| Method |
|---|
| Moist Heat or Steam Sterilization |
Contacts#
| Phone | |
|---|---|
| +1(800)633-8766 | Corporate.UDI@medtronic.com |
Regulatory Flags#
- DUNS number
- 830350380
- Device count
- 1
- DM exempt
- true
- Lot or batch
- true
- Sterilization required before use
- true
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