AFT™ Proximal Humerus Fracture Plate System

FDA UDI

Class II (US FDA UDI)

by Shoulder Options, Inc.

Identity

Trade Name: AFT™ Proximal Humerus Fracture Plate System FDA UDI
Generic Name: Surgical drill guide, reusable FDA UDI
Device Name: 2.7 mm Drill Guide FDA UDI
Model / Reference: SO02-3060 FDA UDI
Description: 2.7 mm Drill Guide FDA UDI

Identifiers

Catalog Number: SO02-3060 FDA UDI
Primary DI / UDI-DI: 00815482020794 FDA UDI
FDA Product Code: HRS FDA UDI
HWC FDA UDI
GMDN Term: Surgical drill guide, reusable FDA UDI

Classification

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

Clinical & Handling

Sterile

FDA UDI

Single Use

FDA UDI

Implantable

FDA UDI

Contains Latex

FDA UDI

Prescription Use

Yes

FDA UDI

Over-the-Counter

FDA UDI

Convenience Kit

FDA UDI

Combination Product

FDA UDI

HCT/P

FDA UDI

Premarket Exempt

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

FDA UDI

Expiration Date

FDA UDI

Manufacturing Date

Yes

FDA UDI

Sterilization Method

Moist Heat or Steam Sterilization FDA UDI

Dimensions & Sizes

Size: Lumen/Inner Diameter — 2.7 Millimeter FDA UDI

Category: Surgical drill guide, reusable

AFT™ Proximal Humerus Fracture Plate System by Shoulder Options, Inc. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

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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: Shoulder Options, Inc.

Sources (1)

FDA UDI ba254875-34fc-49c2-96e1-9833f21b3a3c 36 fields · synced Jun 8, 2026