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Stealth Autoguide™ System

FDA UDI

Class II (US FDA UDI)

by Medtronic Navigation, Inc.

Identity

Trade Name
Stealth Autoguide™ System FDA UDI
Generic Name
Multi-purpose stereotactic surgery system FDA UDI
Device Name
GUIDING INSERT 27586 UPPER AUTOGUIDE FDA UDI
Model / Reference
27586 FDA UDI
Description
GUIDING INSERT 27586 UPPER AUTOGUIDE FDA UDI

Identifiers

Primary DI / UDI-DI
00763000205867 FDA UDI
510(k) Number
K191597 FDA UDI
FDA Product Code
HAW FDA UDI
GMDN Term
Multi-purpose stereotactic surgery system 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

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

No

FDA UDI

Manufacturing Date

No

FDA UDI
Sterilization Method
Moist Heat or Steam Sterilization FDA UDI

Category: Multi-purpose stereotactic surgery system

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

Similar devices

Also classified as Multi-purpose stereotactic surgery system.

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 3f7ac1b7-bc57-479a-a1eb-6b2fb935333e 35 fields · synced May 30, 2026