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StealthStation® AXIEM™ System

FDA UDI

Class II (US FDA UDI)

by Medtronic Navigation, Inc.

Identity

Trade Name
StealthStation® AXIEM™ System FDA UDI
Generic Name
Stereotactic surgery system workstation FDA UDI
Device Name
AXIEM KIT, 9732750, PORTABLE PRE-BUILD FDA UDI
Model / Reference
9732750 FDA UDI
Description
AXIEM KIT, 9732750, PORTABLE PRE-BUILD FDA UDI

Identifiers

Primary DI / UDI-DI
00613994109477 FDA UDI
510(k) Number
K001284 FDA UDI
FDA Product Code
HAW FDA UDI
GMDN Term
Stereotactic surgery system workstation FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
882.4560 FDA UDI
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

No

FDA UDI

Single Use

No

FDA UDI

Implantable

No

FDA UDI

Contains Latex

No

FDA UDI

Prescription Use

Yes

FDA UDI

Over-the-Counter

No

FDA UDI

Convenience Kit

Yes

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

No

FDA UDI

Manufacturing Date

No

FDA UDI

Category: Stereotactic surgery system workstation

StealthStation® AXIEM™ System by Medtronic Navigation, Inc. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Stereotactic surgery system workstation.

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 fe7bcd2d-7c9c-43f5-a8d8-8300ad106cc7 35 fields · synced May 30, 2026