← Back to catalogue

Neofuse

FDA UDI

Class I (US FDA UDI)

by In2bones

Identity

Trade Name
NEOFUSE FDA UDI
Generic Name
Orthopaedic implant aiming arm FDA UDI
Device Name
THUMB WHEEL HIND FOOT PLATE FDA UDI
Model / Reference
P02 00181 FDA UDI
Description
THUMB WHEEL HIND FOOT PLATE FDA UDI

Identifiers

Catalog Number
P02 00181 FDA UDI
Primary DI / UDI-DI
03760225718247 FDA UDI
FDA Product Code
FZX FDA UDI
GMDN Term
Orthopaedic implant aiming arm FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
878.4800 FDA UDI
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

No

FDA UDI

Single Use

No

FDA UDI

Implantable

No

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

No

FDA UDI

Manufacturing Date

No

FDA UDI
Sterilization Method
Moist Heat or Steam Sterilization FDA UDI

Dimensions & Sizes

Size
Width — 13.5 Millimeter FDA UDI
Outer Diameter — 7.5 Millimeter FDA UDI

Category: Orthopaedic implant aiming arm

Neofuse by In2bones — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Orthopaedic implant aiming arm.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

Is this your device? Claim it to add documentation and request validation.

Manufacturer

Manufacturer
In2bones

Sources (1)

  • FDA UDI 2a7f7e79-abfd-40ff-955f-122eb9483c56 36 fields · synced May 31, 2026