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Fusion

FDA UDI

Class II (US FDA UDI)

by Medtronic Navigation, Inc.

Identity

Trade Name
Fusion FDA UDI
Generic Name
Multi-purpose stereotactic surgery system FDA UDI
Device Name
REPLCMT KIT 9735675 FUSION MONITOR FDA UDI
Model / Reference
9735675 FDA UDI
Description
REPLCMT KIT 9735675 FUSION MONITOR FDA UDI

Identifiers

Primary DI / UDI-DI
00643169672390 FDA UDI
510(k) Number
K001284 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

Category: Multi-purpose stereotactic surgery system

Fusion 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 a15e9a22-1d19-4f20-9c0d-bb5402a16521 35 fields · synced May 30, 2026