← Back to catalogue

Freedom

FDA UDI

Class II (US FDA UDI)

by Maxx Orthopedics Inc.

Identity

Trade Name
Freedom FDA UDI
Generic Name
Unicondylar knee prosthesis FDA UDI
Device Name
Partial Femoral Component, Full Post, Size XSmall, Right Medial FDA UDI
Model / Reference
314421 FDA UDI
Description
Partial Femoral Component, Full Post, Size XSmall, Right Medial FDA UDI

Identifiers

Primary DI / UDI-DI
00811767027755 FDA UDI
510(k) Number
K072704 FDA UDI
FDA Product Code
HRY FDA UDI
GMDN Term
Unicondylar knee prosthesis 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

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: Unicondylar knee prosthesis

Freedom by Maxx Orthopedics Inc. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Unicondylar knee prosthesis.

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 9d1d168c-eaea-4200-be7a-d929f1df616e 34 fields · synced May 30, 2026