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Advance®

FDA UDI

Class II (US FDA UDI)

by MicroPort Orthopedics Inc.

Identity

Trade Name
ADVANCE® FDA UDI
Generic Name
Polyethylene patella prosthesis FDA UDI
Device Name
ADVANCE® ONLAY ALL-POLY PATELLA 41mm SINGLE PEG FDA UDI
Model / Reference
KPON41ST FDA UDI
Description
ADVANCE® ONLAY ALL-POLY PATELLA 41mm SINGLE PEG FDA UDI

Identifiers

Catalog Number
KPON41ST FDA UDI
Primary DI / UDI-DI
M684KPON41SP1 FDA UDI
FDA Product Code
JWH FDA UDI
MBH FDA UDI
GMDN Term
Polyethylene patella prosthesis FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
888.3560 FDA UDI
888.3565 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
MRI Safety
MR Conditional FDA UDI

Dimensions & Sizes

Size
Outer Diameter — 41 Millimeter FDA UDI

Category: Polyethylene patella prosthesis

Advance® by MicroPort Orthopedics Inc. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Polyethylene patella prosthesis.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI 11fd6769-994c-4a77-8a9b-2dd0e2c04dcd 36 fields · synced Jun 9, 2026