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Medtronic Navigation

FDA UDI

Class II (US FDA UDI)

by Medtronic Navigation, Inc.

Identity

Trade Name
Medtronic Navigation FDA UDI
Generic Name
Orthopaedic stereotactic surgery system FDA UDI
Device Name
SFW KIT 9735919 S8 SPINE PLAN STAT EU-E FDA UDI
Model / Reference
9735919 FDA UDI
Description
SFW KIT 9735919 S8 SPINE PLAN STAT EU-E FDA UDI

Identifiers

Primary DI / UDI-DI
00763000457433 FDA UDI
510(k) Number
K203639 FDA UDI
FDA Product Code
OLO FDA UDI
GMDN Term
Orthopaedic 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: Orthopaedic stereotactic surgery system

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

Similar devices

Also classified as Orthopaedic 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 c6cb15b8-666a-421f-97fe-53492622136d 35 fields · synced May 30, 2026