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AETOS Shoulder System

FDA UDI

Class II (US FDA UDI)

by Smith & Nephew, Inc.

Identity

Trade Name
AETOS Shoulder System FDA UDI
Generic Name
Coated shoulder humeral stem prosthesis FDA UDI
Device Name
META HUMERAL STEM SIZE 1 SMALL FDA UDI
Model / Reference
STEM-0990-100-001 FDA UDI
Description
META HUMERAL STEM SIZE 1 SMALL FDA UDI

Identifiers

Catalog Number
STEM-0990-100-001 FDA UDI
Primary DI / UDI-DI
00885556814215 FDA UDI
510(k) Number
K220847 FDA UDI
FDA Product Code
KWT FDA UDI
PHX FDA UDI
KWS FDA UDI
HSD FDA UDI
GMDN Term
Coated shoulder humeral stem prosthesis FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
888.3650 FDA UDI
888.3660 FDA UDI
888.3690 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

No

FDA UDI

Category: Coated shoulder humeral stem prosthesis

AETOS Shoulder System by Smith & Nephew, Inc. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Coated shoulder humeral stem prosthesis.

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 e4df31bb-4d1a-43ee-b2d8-a7e71c2d4824 36 fields · synced Jun 8, 2026