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Freedom Knee

FDA UDI

Class II (US FDA UDI)

by Maxx Orthopedics Inc.

Identity

Trade Name
FREEDOM KNEE FDA UDI
Generic Name
Polyethylene patella prosthesis FDA UDI
Device Name
PATELLAR 40 UNIVERSAL FDA UDI
Model / Reference
UPUUX840-K FDA UDI
Description
PATELLAR 40 UNIVERSAL FDA UDI

Identifiers

Primary DI / UDI-DI
00811767021937 FDA UDI
FDA Product Code
JWH FDA UDI
GMDN Term
Polyethylene patella prosthesis FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
888.3560 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
Width — 40 Millimeter FDA UDI
Depth — 8 Millimeter FDA UDI

Category: Polyethylene patella prosthesis

Freedom Knee by Maxx 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 86638393-9a45-420f-924e-016591acfc9c 34 fields · synced May 31, 2026