← Back to catalogue

Journey

FDA UDI

Class II (US FDA UDI)

by Smith & Nephew, Inc.

Identity

Trade Name
JOURNEY FDA UDI
Generic Name
Patella prosthesis trial FDA UDI
Device Name
JOURNEY PATELLA TRIAL BICONVEX 29MM SMALL FDA UDI
Model / Reference
74034529 FDA UDI
Description
JOURNEY PATELLA TRIAL BICONVEX 29MM SMALL FDA UDI

Identifiers

Catalog Number
74034529 FDA UDI
Primary DI / UDI-DI
03596010558893 FDA UDI
510(k) Number
K121393 FDA UDI
FDA Product Code
HRY FDA UDI
GMDN Term
Patella prosthesis trial FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
888.3530 FDA UDI
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

No

FDA UDI

Single Use

No

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

No

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

No

FDA UDI
Sterilization Method
Moist Heat or Steam Sterilization FDA UDI

Category: Patella prosthesis trial

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

Similar devices

Also classified as Patella prosthesis trial.

Cleared under the same submission

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

Is this your device? Claim it to add documentation and request validation.

Manufacturer

Sources (1)

  • FDA UDI 1ff98222-1d02-4bce-b89f-522d5257c699 36 fields · synced Jun 8, 2026