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Freedom Stemmed

FDA UDI

Class II (US FDA UDI)

by Maxx Orthopedics Inc.

Identity

Trade Name
FREEDOM STEMMED FDA UDI
Generic Name
Orthopaedic bone screw, non-bioabsorbable, sterile FDA UDI
Device Name
Augment Screw 10 FDA UDI
Model / Reference
RRUUX412-RK FDA UDI
Description
Augment Screw 10 FDA UDI

Identifiers

Primary DI / UDI-DI
00811767024839 FDA UDI
510(k) Number
K111785 FDA UDI
FDA Product Code
JWH FDA UDI
GMDN Term
Orthopaedic bone screw, non-bioabsorbable, sterile 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

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

Yes

FDA UDI

Manufacturing Date

Yes

FDA UDI
MRI Safety
MR Conditional FDA UDI

Dimensions & Sizes

Size
Length — 10 Millimeter FDA UDI

Category: Orthopaedic bone screw, non-bioabsorbable, sterile

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

Similar devices

Also classified as Orthopaedic bone screw, non-bioabsorbable, sterile.

Cleared under the same submission

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI 2a454ce5-9416-454e-a760-d13bbd1e17cd 35 fields · synced Jun 1, 2026