XRL
- Primary DI
- H981038075340
- Brand
- XRL
- Company
- Synthes GmbH
- Model
- 03.807.534
- Catalog number
- 03807534
- Device description
- XRL MEDIUM TRIAL-ENDPLATE 21MM X 24MM/5 DEG
- Published
- 2015-09-14
- Public version status
- Update
- Distribution status
- In Commercial Distribution
- MRI safety
- Labeling does not contain MRI Safety Information
- Rx
- true
- OTC
- false
- Sterile
- false
- Single use
- false
Contact Domains#
Product Codes#
| Code | Name |
|---|---|
| MQP | SPINAL VERTEBRAL BODY REPLACEMENT DEVICE |
Product Code Classifications#
| Code | Device | Specialty | Class |
|---|---|---|---|
| MQP | Spinal Vertebral Body Replacement Device | Orthopedic | 2 |
Premarket Submissions#
| Submission | Supplement |
|---|---|
| K103320 | 000 |
Premarket Details#
Identifiers And Packaging#
| Identifier | Type | Agency | Package quantity | Status |
|---|---|---|---|---|
| 07611819406643 | Direct Marking | GS1 | 0 | |
| 10705034723662 | Primary | GS1 | 0 | |
| H981038075340 | Secondary | HIBCC | 0 |
Alternate GTIN / UPC / EAN Codes
| Source identifier | GTIN-14 normalized | EAN-13 |
|---|---|---|
| 07611819406643 | 07611819406643 | 7611819406643 |
| 10705034723662 | 10705034723662 |
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 | |
|---|---|
| +1(800)255-2500 | xx@xx.xx |
Regulatory Flags#
- DUNS number
- 486711679
- Device count
- 1
- DM exempt
- false
- 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
- false
- Donation ID number
- false
- Contains natural rubber latex
- false
- No natural rubber latex
- false
- Sterilization required before use
- true
Other Devices From This Company#
| Primary DI | Brand | Model | Catalog | Published |
|---|---|---|---|---|
| 10705034712307 | NA | 03.604.002 | 03604002 | 2016-12-31 |
| 10705034712802 | NA | 03.606.011 | 03606011 | 2016-12-31 |
| 10705034714592 | NA | 03.613.012 | 03613012 | 2016-12-31 |
| 10705034767819 | VentroFix | 304.834 | 304834 | 2016-12-31 |
| 10705034768939 | NA | 314.064 | 314064 | 2016-12-31 |
| 10705034768960 | Click'X | 314.067 | 314067 | 2016-12-31 |
| 10705034768977 | Click'X | 314.068 | 314068 | 2016-12-31 |
| 10705034768984 | Click'X | 314.069 | 314069 | 2016-12-31 |
| 10705034769646 | NA | 328.026 | 328026 | 2016-12-31 |
| 10705034772608 | NA | 388.364 | 388364 | 2016-12-31 |
| 10705034775401 | NA | 389.288 | 389288 | 2016-12-31 |
| 10705034777375 | NA | 394.585 | 394585 | 2016-12-31 |
| 20705034764051 | NA | 292.020 | 292020 | 2019-08-29 |
| 00863176000317 | FIBULINK | FGS-1100 | FGS1100 | 2020-03-26 |
| 00863176000324 | FIBULINK | FGS-1300 | FGS1300 | 2020-03-26 |
| 00863176000300 | FIBULINK | FGS-1000 | FGS1000 | 2017-06-08 |
| 10886982113078 | NA | 04.130.260S | 04130260S | 2016-03-15 |
| 10886982077868 | NA | 03.311.010 | 03311010 | 2015-09-14 |
| 10886982077875 | NA | 03.311.011 | 03311011 | 2015-09-14 |
| 10886982077882 | NA | 03.311.012 | 03311012 | 2015-09-14 |
Other Devices Sharing Product Codes#
| Primary DI | Brand | Company | Product code | Published |
|---|---|---|---|---|
| 00763000857820 | T2 STRATOSPHERE™ Expandable Corpectomy System | MEDTRONIC SOFAMOR DANEK, INC. | MQP | 2026-06-26 |
| 00763000858001 | T2 STRATOSPHERE™ Expandable Corpectomy System | MEDTRONIC SOFAMOR DANEK, INC. | MQP | 2026-06-26 |
| 00840283403460 | LumiVy™ | VY SPINE LLC | MQP | 2026-06-05 |
| 00763000857844 | T2 STRATOSPHERE™ Expandable Corpectomy System | MEDTRONIC SOFAMOR DANEK, INC. | MQP | 2026-06-01 |
| 00763000857943 | T2 STRATOSPHERE™ Expandable Corpectomy System | MEDTRONIC SOFAMOR DANEK, INC. | MQP | 2026-06-01 |
| 00763000857998 | T2 STRATOSPHERE™ Expandable Corpectomy System | MEDTRONIC SOFAMOR DANEK, INC. | MQP | 2026-06-01 |
| 00841732128231 | VALEO VBR | CTL Medical Corporation | MQP | 2023-09-27 |
| 00841732128248 | VALEO VBR | CTL Medical Corporation | MQP | 2023-09-27 |
| 07640172551103 | KONG-TL VBR System, Expansion Handle | icotec AG | MQP | 2020-06-19 |
| 07640172551110 | KONG-TL VBR System, Locking Rod | icotec AG | MQP | 2020-06-19 |
| 08033726407923 | DSC | SINTEA PLUSTEK SRL | MQP | 2015-10-16 |
| 08033726404250 | DSC | SINTEA PLUSTEK SRL | MQP | 2015-10-09 |
| 08033726404267 | DSC | SINTEA PLUSTEK SRL | MQP | 2015-10-09 |
| 08033726407664 | DSC | SINTEA PLUSTEK SRL | MQP | 2015-10-09 |
| 08033726407671 | DSC | SINTEA PLUSTEK SRL | MQP | 2015-10-09 |
| 08033726407701 | DSC | SINTEA PLUSTEK SRL | MQP | 2015-10-09 |
| 08033726407718 | DSC | SINTEA PLUSTEK SRL | MQP | 2015-10-09 |
| 08033726407725 | DSC | SINTEA PLUSTEK SRL | MQP | 2015-10-09 |
| 08033726407732 | DSC | SINTEA PLUSTEK SRL | MQP | 2015-10-09 |
| 08033726407749 | DSC | SINTEA PLUSTEK SRL | MQP | 2015-10-09 |
| 08033726407756 | DSC | SINTEA PLUSTEK SRL | MQP | 2015-10-09 |
| 08033726407763 | DSC | SINTEA PLUSTEK SRL | MQP | 2015-10-09 |
| 08033726407770 | DSC | SINTEA PLUSTEK SRL | MQP | 2015-10-09 |
| 08033726407787 | DSC | SINTEA PLUSTEK SRL | MQP | 2015-10-09 |
| 08033726407794 | DSC | SINTEA PLUSTEK SRL | MQP | 2015-10-09 |
| 08033726407800 | DSC | SINTEA PLUSTEK SRL | MQP | 2015-10-09 |
| 08033726407817 | DSC | SINTEA PLUSTEK SRL | MQP | 2015-10-09 |
| 08033726407824 | DSC | SINTEA PLUSTEK SRL | MQP | 2015-10-09 |
| 08033726407831 | DSC | SINTEA PLUSTEK SRL | MQP | 2015-10-09 |
| 08033726407848 | DSC | SINTEA PLUSTEK SRL | MQP | 2015-10-09 |