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MotoBAND™ CP DynaForce® MPJ Cup and Cone Reamer Kit, 20mm

FDA UDI

Class II (US FDA UDI)

by Crossroads Extremity Systems Llc

Identity

Trade Name
MotoBAND™ CP DynaForce® MPJ Cup and Cone Reamer Kit, 20mm FDA UDI
Generic Name
Surgical instrument handle, non-torque-limiting 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
70CC-0020 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
70CC-0020 FDA UDI
Primary DI / UDI-DI
00815432025961 FDA UDI
510(k) Number
K173710 FDA UDI
FDA Product Code
HWC FDA UDI
HRS FDA UDI
GMDN Term
Surgical instrument handle, non-torque-limiting FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
888.3040 FDA UDI
888.3030 FDA UDI
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

Yes

FDA UDI

Single Use

Yes

FDA UDI

Implantable

No

FDA UDI

Contains Latex

No

FDA UDI

Prescription Use

Yes

FDA UDI

Over-the-Counter

No

FDA UDI

Convenience Kit

Yes

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: Surgical instrument handle, non-torque-limitingBone-resection orthopaedic reamer, single-useBone-resection orthopaedic reamer, reprocessed

MotoBAND™ CP DynaForce® MPJ Cup and Cone Reamer Kit, 20mm by Crossroads Extremity Systems Llc — Class II — FDA UDI — listed in FDA GUDID

Similar devices

Also classified as Bone-resection orthopaedic reamer, reprocessed.

Cleared under the same submission

K173710 also covers:

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Crossroads Extremity Systems Llc

Sources (1)

  • FDA UDI 5e0eb6bf-d407-4acf-938b-397fa9b5e869 36 fields · synced May 31, 2026