IBIS XL
- Primary DI
- 00822409034451
- Brand
- IBIS XL
- Company
- Ortho Development Corporation
- Model
- 752-8575-57A
- Device description
- Diameter 8.5 x 75 mm Cannulated Polyaxial Screw
- Published
- 2017-05-31
- Public version status
- Update
- Distribution status
- In Commercial Distribution
- MRI safety
- Labeling does not contain MRI Safety Information
- Rx
- true
- OTC
- false
- Sterile
- true
- Single use
- true
Related Records
Contact Domains
Product Codes
| Code | Name |
|---|---|
| NKB | Thoracolumbosacral pedicle screw system |
Product Code Classifications
| Code | Device | Specialty | Class |
|---|---|---|---|
| NKB | Thoracolumbosacral Pedicle Screw System | Orthopedic | 2 |
Identifiers And Packaging
| Identifier | Type | Agency | Package quantity | Status |
|---|---|---|---|---|
| 00822409034451 | Primary | GS1 | 0 |
Alternate GTIN / UPC / EAN Codes
| Source identifier | GTIN-14 normalized | UPC-A | EAN-13 |
|---|---|---|---|
| 00822409034451 | 00822409034451 | 822409034451 | 0822409034451 |
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. |
Device Sizes
| Type | Value | Unit |
|---|---|---|
| Length | 75 | Millimeter |
| Outer Diameter | 8.5 | Millimeter |
Sterilization Methods
| Method |
|---|
Contacts
| Phone | |
|---|---|
| +1(801)553-9991 | customerservice@odev.com |
Regulatory Flags
- DUNS number
- 876542390
- 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
- true
- Donation ID number
- false
- Contains natural rubber latex
- false
- No natural rubber latex
- false
- Sterilization required before use
- false
Other Devices From This Company
| Primary DI | Brand | Model | Catalog | Published |
|---|---|---|---|---|
| 00822409131662 | N/A | C-1838-07 | 2026-02-05 | |
| 00822409131679 | N/A | C-1838-08 | 2026-02-05 | |
| 00822409131686 | N/A | C-1838-09 | 2026-02-05 | |
| 00822409131693 | N/A | C-1838-10 | 2026-02-05 | |
| 00822409131709 | N/A | C-1838-11 | 2026-02-05 | |
| 00822409131716 | N/A | C-1838-12 | 2026-02-05 | |
| 00822409131723 | N/A | C-1838-13 | 2026-02-05 | |
| 00822409131730 | N/A | C-1838-14 | 2026-02-05 | |
| 00822409131747 | N/A | C-1838-16 | 2026-02-05 | |
| 00822409131754 | N/A | C-1838-18 | 2026-02-05 | |
| 00822409131761 | N/A | C-1838-20 | 2026-02-05 | |
| 00822409131778 | N/A | C-1839-07 | 2026-02-05 | |
| 00822409131785 | N/A | C-1839-08 | 2026-02-05 | |
| 00822409131792 | N/A | C-1839-09 | 2026-02-05 | |
| 00822409131808 | N/A | C-1839-10 | 2026-02-05 | |
| 00822409131815 | N/A | C-1839-11 | 2026-02-05 | |
| 00822409131822 | N/A | C-1839-12 | 2026-02-05 | |
| 00822409131839 | N/A | C-1839-13 | 2026-02-05 | |
| 00822409131846 | N/A | C-1839-14 | 2026-02-05 | |
| 00822409131853 | N/A | C-1839-16 | 2026-02-05 |
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| 00840185382580 | 4CIS WILL PEDICLE SCREW SYSTEM | SOLCO BIOMEDICAL COMPANY INDIA PRIVATE LIMITED | NKB | 2026-05-25 |
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