Choice Spine SPITFIRE Retractor
- Primary DI
- 00840996168687
- Brand
- Choice Spine SPITFIRE Retractor
- Company
- Choice Spine, LP
- Model
- M070-1007
- Device description
- RETRACTOR,MID BLADE, 70
- Published
- 2019-01-04
- 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 |
|---|---|---|---|---|
| 00840996168687 | Primary | GS1 | 0 |
Alternate GTIN / UPC / EAN Codes
| Source identifier | GTIN-14 normalized | UPC-A | EAN-13 |
|---|---|---|---|
| 00840996168687 | 00840996168687 | 840996168687 | 0840996168687 |
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 |
Contacts#
| Phone | |
|---|---|
| +1(865)246-3333 | info@choicespine.net |
Regulatory Flags#
- DUNS number
- 078293017
- Device count
- 1
- Premarket exempt
- true
- Lot or batch
- true
- Sterilization required before use
- true
Other Devices From This Company#
| Primary DI | Brand | Model | Catalog | Published |
|---|---|---|---|---|
| 00840996183154 | Ambassador | 05-109-18-0027 | 2023-02-03 | |
| 00810211101256 | THUNDERBOLT | M070-0231 | 2026-02-13 | |
| 00840996176552 | BOOMERANG | BT20-D4513 | 2026-01-15 | |
| 00840996176569 | BOOMERANG | BT20-D4515 | 2026-01-15 | |
| 00840996176576 | Boomerang | BT20-D4517 | 2026-01-15 | |
| 00840996176583 | BOOMERANG | B070-0000 | 2026-01-15 | |
| 00840996176590 | BOOMERANG | B070-D010 | 2026-01-15 | |
| 00840996176606 | Boomerang | B070-0001 | 2026-01-15 | |
| 00840996176392 | VEo Lateral | V070-0090 | 2022-11-16 | |
| 00840996176408 | VEo Lateral | V070-0091 | 2022-11-16 | |
| 00840996176415 | VEo Lateral | V070-0092 | 2022-11-16 | |
| 00840996176422 | VEo Lateral | V070-0093 | 2022-11-16 | |
| 00840996176125 | TiGER SHARK Interbody Fusion System | S-PT36-24096 | 2019-01-05 | |
| 00840996176132 | TiGER SHARK Interbody Fusion System | S-PT36-24106 | 2019-01-05 | |
| 00840996176149 | TiGER SHARK Interbody Fusion System | S-PT36-24116 | 2019-01-05 | |
| 00840996176156 | TiGER SHARK Interbody Fusion System | S-PT36-24126 | 2019-01-05 | |
| 00840996176163 | TiGER SHARK Interbody Fusion System | S-PT36-24136 | 2019-01-05 | |
| 00840996176170 | TiGER SHARK Interbody Fusion System | S-PT36-24146 | 2019-01-05 | |
| 00840996176187 | TiGER SHARK Interbody Fusion System | S-PT36-24156 | 2019-01-05 | |
| 00840996176194 | TiGER SHARK Interbody Fusion System | S-PT36-24166 | 2019-01-05 |
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