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Corin Austin Moore Fenestrated Prosthesis (Cobalt Chrome)

FDA UDI

Class II (US FDA UDI)

by Corin Ltd

Identity

Trade Name
Corin Austin Moore Fenestrated Prosthesis (Cobalt Chrome) FDA UDI
Generic Name
Uncoated hip femur prosthesis, one-piece FDA UDI
Device Name
AUSTIN MOORE STANDAR FDA UDI
Model / Reference
108.643 FDA UDI
Description
AUSTIN MOORE STANDAR FDA UDI

Identifiers

Catalog Number
108.643 FDA UDI
Primary DI / UDI-DI
05055196927971 FDA UDI
510(k) Number
K931752 FDA UDI
FDA Product Code
KWL FDA UDI
GMDN Term
Uncoated hip femur prosthesis, one-piece FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
888.3360 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
Sterilization Method
Radiation Sterilization FDA UDI

Category: Uncoated hip femur prosthesis, one-piece

Corin Austin Moore Fenestrated Prosthesis (Cobalt Chrome) by Corin Ltd — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Uncoated hip femur prosthesis, one-piece.

Cleared under the same submission

K931752 also covers:

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Corin Ltd

Sources (1)

  • FDA UDI ae311ffe-9808-4903-ba4d-6e5027926088 36 fields · synced May 31, 2026