VyPlate™
- Primary DI
- 00840283407949
- Brand
- VyPlate™
- Company
- VY SPINE LLC
- Model
- 06-IPH-002
- Device description
- Side Angled Plate Holder
- Published
- 2026-06-05
- Public version status
- New
- Distribution status
- In Commercial Distribution
- MRI safety
- MR Unsafe
- Rx
- true
- OTC
- false
- Sterile
- false
- Single use
- false
Contact Domains#
Product Codes#
| Code | Name |
|---|---|
| KWQ | Appliance, Fixation, Spinal Intervertebral Body |
Product Code Classifications#
| Code | Device | Specialty | Class |
|---|---|---|---|
| KWQ | Appliance, Fixation, Spinal Intervertebral Body | Orthopedic | 2 |
Premarket Submissions#
| Submission | Supplement |
|---|---|
| K221572 | 000 |
Premarket Details#
Identifiers And Packaging#
| Identifier | Type | Agency | Package quantity | Status |
|---|---|---|---|---|
| 00840283407949 | Primary | GS1 | 0 |
Alternate GTIN / UPC / EAN Codes
| Source identifier | GTIN-14 normalized | UPC-A | EAN-13 |
|---|---|---|---|
| 00840283407949 | 00840283407949 | 840283407949 | 0840283407949 |
GMDN Terms#
| Term | Definition |
|---|---|
| Internal spinal fixation procedure kit, reusable | A collection of various orthopaedic manual surgical instruments (e.g., screwdriver, trial rod, adaptor, mallet, guide tube, chisel, rasp, awl, burr, tap, drill) intended to be used to perform a bone-screw internal spinal fixation and/or spinal fusion cage implantation procedure (including stereotactic procedures); implanted devices are not included. This is a reusable device. |
Sterilization Methods#
| Method |
|---|
| Moist Heat or Steam Sterilization |
Contacts#
| Phone | |
|---|---|
| 866-489-7746 | info@vyspine.com |
Regulatory Flags#
- DUNS number
- 049592888
- 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 |
|---|---|---|---|---|
| 00840283403460 | LumiVy™ | 03-T-0927-0-06-PET-R | 2026-06-05 | |
| 00840283403897 | VySpan™ | 05-CRR7-3535-TI-N | 2026-06-05 | |
| 00840283403927 | VySpan™ | 05-CRR10-3540-TI-N | 2026-06-05 | |
| 00840283403477 | LumiVy™ | 03-T-0927-0-07-PET-R | 2026-04-30 | |
| 00840283403484 | LumiVy™ | 03-T-0927-0-08-PET-R | 2026-04-30 | |
| 00840283403491 | LumiVy™ | 03-T-0927-0-09-PET-R | 2026-04-30 | |
| 00840283403507 | LumiVy™ | 03-T-0927-0-10-PET-R | 2026-04-30 | |
| 00840283403514 | LumiVy™ | 03-T-0927-0-11-PET-R | 2026-04-29 | |
| 00840283403521 | LumiVy™ | 03-T-0927-0-12-PET-R | 2026-04-28 | |
| 00840283403538 | LumiVy™ | 03-T-0927-0-13-PET-R | 2026-04-28 | |
| 00840283403545 | LumiVy™ | 03-T-0927-0-14-PET-R | 2026-04-28 | |
| 00840283403552 | LumiVy™ | 03-T-0927-0-15-PET-R | 2026-04-28 | |
| 00840283403576 | LumiVy™ | 03-A-3427-6-09-PET-R | 2026-04-27 | |
| 00840283403583 | LumiVy™ | 03-A-3427-6-10-PET-R | 2026-04-27 | |
| 00840283403590 | LumiVy™ | 03-A-3427-6-11-PET-R | 2026-04-27 | |
| 00840283403606 | LumiVy™ | 03-A-3427-6-12-PET-R | 2026-04-27 | |
| 00840283403613 | LumiVy™ | 03-A-3427-6-13-PET-R | 2026-04-27 | |
| 00840283403620 | LumiVy™ | 03-A-3427-6-14-PET-R | 2026-04-27 | |
| 00840283403569 | LumiVy™ | 03-A-3427-6-08-PET-R | 2026-04-24 | |
| 00840283404139 | ClariVy™ | 02-ITL-1210-08 | 2026-04-24 |
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| Primary DI | Brand | Company | Product code | Published |
|---|---|---|---|---|
| 00763000786458 | CD HORIZON® Fenestrated Screw Spinal System | MEDTRONIC SOFAMOR DANEK, INC. | KWQ | 2026-10-15 |
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