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StealthFix Intraosseous Fixation System

FDA UDI

Class II (US FDA UDI)

by Medartis Inc.

Identity

Trade Name
StealthFix Intraosseous Fixation System FDA UDI
Generic Name
Orthopaedic bone screw (non-sliding) FDA UDI
Device Name
StealthFix Fully Threaded Headed Screw Size 20 FDA UDI
Model / Reference
SF3620 FDA UDI
Description
StealthFix Fully Threaded Headed Screw Size 20 FDA UDI

Identifiers

Primary DI / UDI-DI
00810082898019 FDA UDI
510(k) Number
K232324 FDA UDI
FDA Product Code
HWC FDA UDI
GMDN Term
Orthopaedic bone screw (non-sliding) FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
888.3040 FDA UDI
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

No

FDA UDI

Single Use

Yes

FDA UDI

Implantable

Yes

FDA UDI

Contains Latex

No

FDA UDI

Prescription Use

No

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
Sterilization Method
Moist Heat or Steam Sterilization FDA UDI

Category: Orthopaedic bone screw (non-sliding)

StealthFix Intraosseous Fixation System by Medartis Inc. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Orthopaedic bone screw (non-sliding).

Cleared under the same submission

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Medartis Inc.

Sources (1)

  • FDA UDI 564f01e1-5913-445e-adf2-8d0f4be31ac9 34 fields · synced May 30, 2026