PLIF Interbody
- Primary DI
- 00195860009048
- Brand
- PLIF Interbody
- Company
- Evolution Spine LLC
- Model
- P-1112
- Catalog number
- P-1112
- Device description
- PLIF Trial 12mm Lordotic
- Published
- 2021-06-12
- Public version status
- Update
- Distribution status
- In Commercial Distribution
- MRI safety
- Labeling does not contain MRI Safety Information
- Rx
- true
Contact Domains#
Product Codes#
| Code | Name |
|---|---|
| LXH | ORTHOPEDIC MANUAL SURGICAL INSTRUMENT |
Product Code Classifications#
| Code | Device | Specialty | Class |
|---|---|---|---|
| LXH | Orthopedic Manual Surgical Instrument | Orthopedic | 1 |
Identifiers And Packaging#
| Identifier | Type | Agency | Package quantity | Status |
|---|---|---|---|---|
| 00195860009048 | Primary | GS1 | 0 |
Alternate GTIN / UPC / EAN Codes
| Source identifier | GTIN-14 normalized | UPC-A | EAN-13 |
|---|---|---|---|
| 00195860009048 | 00195860009048 | 195860009048 | 0195860009048 |
GMDN Terms#
| Term | Definition |
|---|---|
| Surgical implant/trial-implant/sizer holder, reusable | A hand-held manual surgical instrument designed to connect to and hold an implant (e.g., bone screw, bone graft), trial implant, or implantable device sizer/template (e.g., glenoid defect sizer, hearing implant template) to facilitate guidance, gauging/sizing, and/or monitoring of the held device during orthopaedic or ear/nose/throat (ENT) surgery. The instrument is typically made of metal or synthetic polymer materials and is typically constructed in the form of a long shaft with a handle at the proximal end and a device holding/fixation mechanism at the distal end. This is a reusable device. |
Device Sizes#
| Type | Value | Unit |
|---|---|---|
| Device Size Text, specify | 0 | |
| Height | 12 | Millimeter |
Sterilization Methods#
| Method |
|---|
| Moist Heat or Steam Sterilization |
Contacts#
| Phone | |
|---|---|
| +1(214)682-8536 | info@evolutionspine.com |
Regulatory Flags#
- DUNS number
- 116940934
- Device count
- 1
- DM exempt
- true
- Premarket exempt
- true
- Lot or batch
- true
- Sterilization required before use
- true
Other Devices From This Company#
| Primary DI | Brand | Model | Catalog | Published |
|---|---|---|---|---|
| 00195860023112 | EMERGE Anterior Cervical Plate System | 100-A068 | 100-A068 | 2023-08-21 |
| 00195860014042 | EMERGE Anterior Cervical Plate System | 100-A024 | 100-A024 | 2021-11-01 |
| 00195860014059 | EMERGE Anterior Cervical Plate System | 100-A025 | 100-A025 | 2021-11-01 |
| 00195860010457 | Skye Cervical Plate System | CP-1007 | CP-1007 | 2021-06-02 |
| 00195860031803 | E3D-C Interbody System | 130-A129 | 130-A129 | 2026-02-20 |
| 00195860031810 | E3D-C Interbody System | 130-A130 | 130-A130 | 2026-02-20 |
| 00195860031827 | E3D-C Interbody System | 130-A131 | 130-A131 | 2026-02-20 |
| 00195860031834 | E3D-C Interbody System | 130-A132 | 130-A132 | 2026-02-20 |
| 00195860031841 | E3D-C Interbody System | 130-A133 | 130-A133 | 2026-02-20 |
| 00195860031858 | E3D-C Interbody System | 130-A134 | 130-A134 | 2026-02-20 |
| 00195860031865 | E3D-C Interbody System | 130-A135 | 130-A135 | 2026-02-20 |
| 00195860031872 | E3D-C Interbody System | 130-A136 | 130-A136 | 2026-02-20 |
| 00195860031889 | E3D-C Interbody System | 130-A137 | 130-A137 | 2026-02-20 |
| 00195860031896 | E3D-C Interbody System | 130-A138 | 130-A138 | 2026-02-20 |
| 00195860031902 | E3D-C Interbody System | 130-A139 | 130-A139 | 2026-02-20 |
| 00195860031919 | E3D-C Interbody System | 130-A140 | 130-A140 | 2026-02-20 |
| 00195860031926 | E3D-C Interbody System | 130-A141 | 130-A141 | 2026-02-20 |
| 00195860031933 | E3D-C Interbody System | 130-A142 | 130-A142 | 2026-02-20 |
| 00195860031940 | E3D-C Interbody System | 130-A143 | 130-A143 | 2026-02-20 |
| 00195860031957 | E3D-C Interbody System | 130-A144 | 130-A144 | 2026-02-20 |
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