Identity
- Trade Name
- MotoBAND™ CP DynaForce® MPJ FDA UDI
- Generic Name
- Orthopaedic bone staple, non-adjustable FDA UDI
- Device Name
- 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. FDA UDI
- Model / Reference
- MPJ Short 5deg Valgus/5deg Dorsiflexion FDA UDI
- 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. FDA UDI
Identifiers
- Catalog Number
- 7150-5018 FDA UDI
- Primary DI / UDI-DI
- 00815432026371 FDA UDI
- 510(k) Number
- K173710 FDA UDI
- FDA Product Code
- HWC FDA UDIHRS FDA UDI
- GMDN Term
- Orthopaedic bone staple, non-adjustable FDA UDI
Classification
- Device Class
- Class II FDA UDI
- Regulation Number
- 888.3040 FDA UDI888.3030 FDA UDI
- Commercial Distribution
- In Commercial Distribution FDA UDI
Clinical & Handling
Sterile
Yes
FDA UDI
Single Use
Yes
FDA UDI
Implantable
Yes
FDA UDI
Contains Latex
No
FDA UDI
Prescription Use
Yes
FDA UDI
Over-the-Counter
No
FDA UDI
Convenience Kit
No
FDA UDI
Combination Product
No
FDA UDI
HCT/P
No
FDA UDI
Premarket Exempt
No
FDA UDI
Lot / Batch Number
Yes
FDA UDI
Serial Number
No
FDA UDI
Expiration Date
Yes
FDA UDI
Manufacturing Date
No
FDA UDI
Category: Orthopaedic fixation plate, non-bioabsorbableOrthopaedic bone staple, non-adjustable
MotoBAND™ CP DynaForce® MPJ by Crossroads Extremity Systems Llc — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS
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Cleared under the same submission
K173710 also covers:
- MotoBAND — CROSSROADS EXTREMITY SYSTEMS LLC
- MotoBAND — CROSSROADS EXTREMITY SYSTEMS LLC
- MotoBAND — CROSSROADS EXTREMITY SYSTEMS LLC
- MotoBAND — CROSSROADS EXTREMITY SYSTEMS LLC
- MotoBAND — CROSSROADS EXTREMITY SYSTEMS LLC
- MotoBAND — CROSSROADS EXTREMITY SYSTEMS LLC
- MotoBAND — CROSSROADS EXTREMITY SYSTEMS LLC
- MotoBAND — CROSSROADS EXTREMITY SYSTEMS LLC
- MotoBAND — CROSSROADS EXTREMITY SYSTEMS LLC
- MotoBAND — CROSSROADS EXTREMITY SYSTEMS LLC
- MotoBAND — CROSSROADS EXTREMITY SYSTEMS LLC
- MotoBAND — CROSSROADS EXTREMITY SYSTEMS LLC
Authorization Coverage (1 country)
Regulatory Authorizations
United States Pending data
FDA UDI
| Source | Region | Type | Cert / Approval No. | Class | Status |
|---|---|---|---|---|---|
| FDA UDI | United States | FDA UDI | Registered in GUDID | Class II | Pending data |
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Manufacturer
- Manufacturer
- Crossroads Extremity Systems Llc
Sources (1)
- FDA UDI 276d5c74-fce9-43f8-a5e7-1432d18ba92a 36 fields · synced May 30, 2026