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Katalyst™ Bipolar Radial Head System

FDA UDI

Class II (US FDA UDI)

by Ascension Orthopedics, Inc.

Identity

Trade Name
Katalyst™ Bipolar Radial Head System FDA UDI
Generic Name
Elbow radius prosthesis FDA UDI
Device Name
The Katalyst Radial Head restores the support and bearing surfaces of the radial head in the face of fracture, arthritis or failed prior implantation. FDA UDI
Model / Reference
221418 FDA UDI
Description
The Katalyst Radial Head restores the support and bearing surfaces of the radial head in the face of fracture, arthritis or failed prior implantation. FDA UDI

Identifiers

Catalog Number
221418 FDA UDI
Primary DI / UDI-DI
10381780065784 FDA UDI
510(k) Number
K032806 FDA UDI
FDA Product Code
KWI FDA UDI
GMDN Term
Elbow radius prosthesis FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
888.3170 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: Elbow radius prosthesis

Katalyst™ Bipolar Radial Head System by Ascension Orthopedics, Inc. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Elbow radius 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 4b18fb13-d246-47dd-b5c7-037114da003b 39 fields · synced Jun 8, 2026