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Xtendobutton

FDA UDI

Class I (US FDA UDI)

by Smith & Nephew, Inc.

Identity

Trade Name
XTENDOBUTTON FDA UDI
Generic Name
Ligament bone anchor FDA UDI
Device Name
XTENDOBUTTON Round Large 21 mm DIA 10 mm peg FDA UDI
Model / Reference
71935603 FDA UDI
Description
XTENDOBUTTON Round Large 21 mm DIA 10 mm peg FDA UDI

Identifiers

Catalog Number
71935603 FDA UDI
Primary DI / UDI-DI
00885556702710 FDA UDI
FDA Product Code
KGS FDA UDI
GMDN Term
Ligament bone anchor FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
878.4930 FDA UDI
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

Yes

FDA UDI

Single Use

Yes

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

Yes

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

Yes

FDA UDI

Manufacturing Date

No

FDA UDI

Category: Ligament bone anchor

Xtendobutton by Smith & Nephew, Inc. — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Ligament bone anchor.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI d0573c40-b255-4bf1-81dd-07fdc4ad2884 35 fields · synced Jun 6, 2026