Reform Pedicle Screw System
- Primary DI
- 00840019900423
- Brand
- Reform Pedicle Screw System
- Company
- PRECISION SPINE, INC.
- Model
- 39-PA-8500
- Catalog number
- 39-PA-8500
- Device description
- ø8.5 x 100 mm POLYAXIAL SCREW
- Published
- 2019-05-21
- Public version status
- Update
- Distribution status
- In Commercial Distribution
- MRI safety
- Labeling does not contain MRI Safety Information
- Rx
- true
- Single use
- true
Product Codes#
Product Code Classifications#
| Code | Device | Specialty | Class |
|---|---|---|---|
| KWP | Appliance, Fixation, Spinal Interlaminal | Orthopedic | 2 |
| MNH | Orthosis, Spondylolisthesis Spinal Fixation | Orthopedic | 2 |
| MNI | Orthosis, Spinal Pedicle Fixation | Orthopedic | 2 |
| NKB | Thoracolumbosacral Pedicle Screw System | Orthopedic | 2 |
| OSH | Pedicle Screw Spinal System, Adolescent Idiopathic Scoliosis | Orthopedic | 2 |
Premarket Submissions#
| Submission | Supplement |
|---|---|
| K143248 | 000 |
Premarket Details#
Identifiers And Packaging#
| Identifier | Type | Agency | Package quantity | Status |
|---|---|---|---|---|
| 00840019900423 | Primary | GS1 | 0 |
Alternate GTIN / UPC / EAN Codes
| Source identifier | GTIN-14 normalized | UPC-A | EAN-13 |
|---|---|---|---|
| 00840019900423 | 00840019900423 | 840019900423 | 0840019900423 |
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. |
Sterilization Methods#
| Method |
|---|
| Moist Heat or Steam Sterilization |
Regulatory Flags#
- DUNS number
- 079398589
- Device count
- 1
- DM exempt
- true
- Sterilization required before use
- true
Other Devices From This Company#
| Primary DI | Brand | Model | Catalog | Published |
|---|---|---|---|---|
| 00840019970907 | MD-Vue™ Lateral Access System | 54-TA-0500 | 54-TA-0500 | 2026-05-01 |
| 00840019970914 | MD-Vue™ Lateral Access System | 54-TA-0600 | 54-TA-0600 | 2026-05-01 |
| 00840019970921 | MD-Vue™ Lateral Access System | 54-TA-0700 | 54-TA-0700 | 2026-05-01 |
| 00840019970938 | MD-Vue™ Lateral Access System | 54-TA-0800 | 54-TA-0800 | 2026-05-01 |
| 00840019970945 | MD-Vue™ Lateral Access System | 54-TA-0900 | 54-TA-0900 | 2026-05-01 |
| 00840019970952 | MD-Vue™ Lateral Access System | 54-TA-1000 | 54-TA-1000 | 2026-05-01 |
| 00840019971133 | Reform Ti Modular | 39-SF-6545 | 39-SF-6545 | 2026-01-13 |
| 00840019971140 | Reform Ti Modular | 39-SF-6550 | 39-SF-6550 | 2026-01-13 |
| 00840019971157 | Reform Ti Modular | 39-SF-6555 | 39-SF-6555 | 2026-01-13 |
| 00840019971164 | Reform Ti Modular | 39-SF-6560 | 39-SF-6560 | 2026-01-13 |
| 00840019971171 | Reform Ti Modular | 39-SF-7530 | 39-SF-7530 | 2026-01-13 |
| 00840019971188 | Reform Ti Modular | 39-SF-7535 | 39-SF-7535 | 2026-01-13 |
| 00840019971195 | Reform Ti Modular | 39-SF-7540 | 39-SF-7540 | 2026-01-13 |
| 00840019971201 | Reform Ti Modular | 39-SF-7545 | 39-SF-7545 | 2026-01-13 |
| 00840019971218 | Reform Ti Modular | 39-SF-7550 | 39-SF-7550 | 2026-01-13 |
| 00840019971225 | Reform Ti Modular | 39-SF-7555 | 39-SF-7555 | 2026-01-13 |
| 00840019971232 | Reform Ti Modular | 39-SF-7560 | 39-SF-7560 | 2026-01-13 |
| 00840019971249 | Reform Ti Modular | 39-SF-7570 | 39-SF-7570 | 2026-01-13 |
| 00840019971256 | Reform Ti Modular | 39-SF-7580 | 39-SF-7580 | 2026-01-13 |
| 00840019971263 | Reform Ti Modular | 39-SF-8535 | 39-SF-8535 | 2026-01-13 |
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