OIC Lumbar Interbody Cages
- Primary DI
- M696110070
- Brand
- OIC Lumbar Interbody Cages
- Company
- ORTHOPAEDIC IMPLANT COMPANY, THE
- Model
- 110-07
- Device description
- LUMBAR IMPLANT TRIAL 7MM CRESCENT
- Published
- 2017-02-01
- 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 |
|---|---|
| MAX | Intervertebral Fusion Device With Bone Graft, Lumbar |
Product Code Classifications#
| Code | Device | Specialty | Class |
|---|---|---|---|
| MAX | Intervertebral Fusion Device With Bone Graft, Lumbar | Orthopedic | 2 |
Premarket Submissions#
| Submission | Supplement |
|---|---|
| K082260 | 000 |
Premarket Details#
Identifiers And Packaging#
| Identifier | Type | Agency | Package quantity | Status |
|---|---|---|---|---|
| M696110070 | Primary | HIBCC | 0 |
GMDN Terms#
| Term | Definition |
|---|---|
| Spinal implant trial | A copy of a final spinal prosthesis, graft, or other implantable spinal device (e.g., may include intervertebral disc prosthesis, spinal cage, spinal hook) used to validate the proper size of the permanent implant required by the patient, to determine its appropriate position, and/or to verify that the implant site has been cut to the proper dimensions. It can be made of metal or plastic. This is a reusable device. |
Sterilization Methods#
| Method |
|---|
| Moist Heat or Steam Sterilization |
Contacts#
| Phone | |
|---|---|
| 775 636 8281 | Info@OrthoImplantCompany.com |
Regulatory Flags#
- DUNS number
- 070061160
- Device count
- 1
- Lot or batch
- true
- Manufacturing date on label
- true
- Sterilization required before use
- true
Other Devices From This Company#
| Primary DI | Brand | Model | Catalog | Published |
|---|---|---|---|---|
| 10811998032150 | OIC Cannulated Screw System | 01-SHS10 | 2018-07-31 | |
| 10811998036301 | OIC Intramedullary Nail System | 01-IM30 | 2018-07-31 | |
| 10811998036325 | OIC Intramedullary Nail System | 01-IM32 | 2018-07-31 | |
| 10811998036349 | OIC Intramedullary Nail System | 01-IM34 | 2018-07-31 | |
| 10811998036387 | OIC Intramedullary Nail System | 01-IM40 | 2018-07-31 | |
| 10811998036394 | OIC Intramedullary Nail System | 01-IM41 | 2018-07-31 | |
| 10811998036561 | OIC Intramedullary Nail System | 01-IM58 | 2018-08-07 | |
| 10811998038022 | OIC Intramedullary Nail System | 01-IMSE03 | 2018-08-07 | |
| 10811998038039 | OIC Intramedullary Nail System | 01-IMSE04 | 2018-08-07 | |
| M69601IM300 | OIC Intramedullary Nail System | 01-IM30 | 2017-02-01 | |
| M69601IM320 | OIC Intramedullary Nail System | 01-IM32 | 2017-02-01 | |
| M69601IM340 | OIC Intramedullary Nail System | 01-IM34 | 2017-02-01 | |
| M69601IM400 | OIC Intramedullary Nail System | 01-IM40 | 2017-02-01 | |
| M69601IM410 | OIC Intramedullary Nail System | 01-IM41 | 2017-02-01 | |
| M69601SHS100 | OIC Cannulated Screw System | 01-SHS10 | 2017-02-01 | |
| 10811998039555 | OIC Variable Angle Small Fragment Locking Plate System | 01-SF27 | 2023-09-06 | |
| 10811998033478 | OIC Variable Angle Small Fragment Locking Plate System | 01-SF11 | 2018-07-31 | |
| 10811998033485 | OIC Variable Angle Small Fragment Locking Plate System | 01-SF12 | 2018-07-31 | |
| M69601SF110 | OIC Variable Angle Small Fragment Locking Plate System | 01-SF11 | 2017-02-01 | |
| M69601SF120 | OIC Variable Angle Small Fragment Locking Plate System | 01-SF12 | 2017-02-01 |
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|---|---|---|---|---|
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| B707125355730600 | DUALX DUAL PORTAL DISPOSABLE KIT-60MM (USA) | AMPLIFY SURGICAL, INC. | MAX | 2026-09-04 |
| B707125355730700 | DUALX DUAL PORTAL DISPOSABLE KIT-70MM (USA) | AMPLIFY SURGICAL, INC. | MAX | 2026-09-04 |
| B707125355730800 | DUALX DUAL PORTAL DISPOSABLE KIT-80MM (USA) | AMPLIFY SURGICAL, INC. | MAX | 2026-09-04 |
| B707125355730900 | DUALX DUAL PORTAL DISPOSABLE KIT-90MM (USA) | AMPLIFY SURGICAL, INC. | MAX | 2026-09-04 |
| B707125355731000 | DUALX DUAL PORTAL DISPOSABLE KIT-100MM (USA) | AMPLIFY SURGICAL, INC. | MAX | 2026-09-04 |
| B707125355731100 | DUALX DUAL PORTAL DISPOSABLE KIT-110MM (USA) | AMPLIFY SURGICAL, INC. | MAX | 2026-09-04 |
| B707125355731200 | DUALX DUAL PORTAL DISPOSABLE KIT-120MM (USA) | AMPLIFY SURGICAL, INC. | MAX | 2026-09-04 |
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| 00763000703936 | MSB CAPSTONE CONTROL™ Spinal System | MEDTRONIC SOFAMOR DANEK, INC. | MAX | 2026-08-27 |
| 00763000703950 | MSB CAPSTONE CONTROL™ Spinal System | MEDTRONIC SOFAMOR DANEK, INC. | MAX | 2026-08-27 |
| 00763000703967 | MSB CAPSTONE CONTROL™ Spinal System | MEDTRONIC SOFAMOR DANEK, INC. | MAX | 2026-08-27 |
| 00763000703981 | MSB CAPSTONE CONTROL™ Spinal System | MEDTRONIC SOFAMOR DANEK, INC. | MAX | 2026-08-27 |
| 00763000703998 | MSB CAPSTONE CONTROL™ Spinal System | MEDTRONIC SOFAMOR DANEK, INC. | MAX | 2026-08-27 |
| 00763000704001 | MSB CAPSTONE CONTROL™ Spinal System | MEDTRONIC SOFAMOR DANEK, INC. | MAX | 2026-08-27 |
| 00763000704018 | MSB CAPSTONE CONTROL™ Spinal System | MEDTRONIC SOFAMOR DANEK, INC. | MAX | 2026-08-27 |
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| 00763000704032 | MSB CAPSTONE CONTROL™ Spinal System | MEDTRONIC SOFAMOR DANEK, INC. | MAX | 2026-08-27 |
| 00763000704049 | MSB CAPSTONE CONTROL™ Spinal System | MEDTRONIC SOFAMOR DANEK, INC. | MAX | 2026-08-27 |
| 00763000704063 | MSB CAPSTONE CONTROL™ Spinal System | MEDTRONIC SOFAMOR DANEK, INC. | MAX | 2026-08-27 |
| 00763000704070 | MSB CAPSTONE CONTROL™ Spinal System | MEDTRONIC SOFAMOR DANEK, INC. | MAX | 2026-08-27 |
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| 00763000704148 | MSB CAPSTONE CONTROL™ Spinal System | MEDTRONIC SOFAMOR DANEK, INC. | MAX | 2026-08-27 |
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