MotoBAND™ CP DynaForce® MPJ Cup and Cone Reamer Kit, 22mm
- Primary DI
- 00815432025978
- Brand
- MotoBAND™ CP DynaForce® MPJ Cup and Cone Reamer Kit, 22mm
- Company
- CROSSROADS EXTREMITY SYSTEMS
- Model
- 70CC-0022
- Catalog number
- 70CC-0022
- Device description
- The MotoBAND™ CP DynaForce® MPJ Implant System is a bone plating system indicated for stabilization and fixation of fresh fractures, revision procedures, joint fusion and reconstruction of small bones of the hand, feet, wrist, ankles, fingers and toes. It consist of plates and screws. Certain plates in the system are compatible with the MotoCLIP/DynaForce Superelastic Fixation System.
- Published
- 2018-04-24
- Public version status
- Update
- Distribution status
- In Commercial Distribution
- MRI safety
- Labeling does not contain MRI Safety Information
- Rx
- true
- Sterile
- true
- Single use
- true
Contact Domains#
Product Codes#
Product Code Classifications#
Premarket Submissions#
| Submission | Supplement |
|---|---|
| K173710 | 000 |
Premarket Details#
Identifiers And Packaging#
| Identifier | Type | Agency | Package quantity | Status |
|---|---|---|---|---|
| 00815432025978 | Primary | GS1 | 0 |
Alternate GTIN / UPC / EAN Codes
| Source identifier | GTIN-14 normalized | UPC-A | EAN-13 |
|---|---|---|---|
| 00815432025978 | 00815432025978 | 815432025978 | 0815432025978 |
GMDN Terms#
| Term | Definition |
|---|---|
| Bone-resection orthopaedic reamer, reprocessed | A sterile, orthopaedic, surgical instrument designed to resect (cut out part of the bone) and precisely shape a specific area of bone for the acceptance of a prosthetic implant, typically at or within a joint (e.g., condyle of knee, neck of humerus, olecranon of ulna). Commonly called a mill or a reamer it is typically designed as either a preshaped or a solid cylindrical body with an end/circumferential cutting edge, and is attached to a shaft for manual or powered rotation. It is typically made of a high-grade stainless steel alloy available in varying sizes. This is a previously used single-use device that has been processed for an additional single-use patient application. |
Sterilization Methods#
| Method |
|---|
Contacts#
| Phone | |
|---|---|
| 901-221-8406 | info@crextremity.com |
Regulatory Flags#
- DUNS number
- 058864308
- Device count
- 1
- DM exempt
- true
- Premarket exempt
- true
- Kit
- true
- Lot or batch
- true
- Expiration date on label
- true
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