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FO Micro Screw System

FDA UDI

Class I (US FDA UDI)

by Field Orthopaedics Pty Ltd

Identity

Trade Name
FO Micro Screw System FDA UDI
Generic Name
Surgical drill guide, reusable FDA UDI
Device Name
FO Soft Tissue Protector FDA UDI
Model / Reference
MSTP-0000 FDA UDI
Description
FO Soft Tissue Protector FDA UDI

Identifiers

Catalog Number
MSTP-0000/1 FDA UDI
Primary DI / UDI-DI
09353903000303 FDA UDI
510(k) Number
K180348 FDA UDI
FDA Product Code
LXH FDA UDI
GMDN Term
Surgical drill guide, reusable FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
888.4540 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

Category: Surgical drill guide, reusable

FO Micro Screw System by Field Orthopaedics Pty Ltd — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Surgical drill guide, reusable.

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 09361a97-128b-4066-9c72-2d0ad6ea42b9 35 fields · synced May 30, 2026