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FuzeFix Mini

FDA UDI

Class II (US FDA UDI)

by Fusion Orthopedics, Llc

Identity

Trade Name
FuzeFix Mini FDA UDI
Generic Name
Implantable bone washer FDA UDI
Device Name
FX Mini 4.0mm Smooth Washer FDA UDI
Model / Reference
FX-HD-4000-S FDA UDI
Description
FX Mini 4.0mm Smooth Washer FDA UDI

Identifiers

Primary DI / UDI-DI
00840124514065 FDA UDI
510(k) Number
K170038 FDA UDI
FDA Product Code
HTN FDA UDI
GMDN Term
Implantable bone washer FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
888.3030 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

Yes

FDA UDI

Category: Implantable bone washer

FuzeFix Mini by Fusion Orthopedics, Llc — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Implantable bone washer.

Cleared under the same submission

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI 0563dc63-7741-4096-bb08-1dfefe606a91 34 fields · synced May 29, 2026