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.
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- Geniant Cranial — Koh Young Technology, Inc. · Class II
- StealthStation® AXIEM™ System — MEDTRONIC NAVIGATION, INC. · Class II
- Synergy — MEDTRONIC NAVIGATION, INC. · Class II
- Stealthstation® S7™ — MEDTRONIC NAVIGATION, INC. · Class II
Cleared under the same submission
K001284 also covers:
- AXIEM™ — MEDTRONIC NAVIGATION, INC.
- AXIEM™ — MEDTRONIC NAVIGATION, INC.
- AxiEM™ — MEDTRONIC NAVIGATION, INC.
- AxiEM™ — MEDTRONIC NAVIGATION, INC.
- AxiEM™ — MEDTRONIC NAVIGATION, INC.
- AxiEM™ — MEDTRONIC NAVIGATION, INC.
- Fusion — MEDTRONIC NAVIGATION, INC.
- Fusion™ ENT Image Guidance System — MEDTRONIC NAVIGATION, INC.
- Fusion™ ENT Image Guidance System — MEDTRONIC NAVIGATION, INC.
- Fusion™ ENT Image Guidance System — MEDTRONIC NAVIGATION, INC.
Authorization Coverage (1 country)
Regulatory Authorizations
United States Pending data
FDA UDI
| Source | Region | Type | Cert / Approval No. | Class | Status |
|---|---|---|---|---|---|
| FDA UDI | United States | FDA UDI | Registered in GUDID | Class II | Pending data |
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Manufacturer
- Manufacturer
- Medtronic Navigation, Inc.
Sources (1)
- FDA UDI fe7bcd2d-7c9c-43f5-a8d8-8300ad106cc7 35 fields · synced May 30, 2026