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Rialto™ Si Fusion System

FDA UDI

Class I (US FDA UDI)

by Medtronic Sofamor Danek, Inc.

Identity

Trade Name
RIALTO™ SI FUSION SYSTEM FDA UDI
Generic Name
Surgical screwdriver, reusable FDA UDI
Device Name
DRIVER NAV7426001 SCREW RIALTO FDA UDI
Model / Reference
NAV7426001 FDA UDI
Description
DRIVER NAV7426001 SCREW RIALTO FDA UDI

Identifiers

Primary DI / UDI-DI
00643169571808 FDA UDI
510(k) Number
K161210 FDA UDI
FDA Product Code
HWE FDA UDI
OLO FDA UDI
OUR FDA UDI
GMDN Term
Surgical screwdriver, reusable FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
878.4820 FDA UDI
882.4560 FDA UDI
888.3040 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: Surgical screwdriver, reusable

Rialto™ Si Fusion System by Medtronic Sofamor Danek, Inc. — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Surgical screwdriver, reusable.

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 a9f0b2ef-7e5f-4418-9753-6e2f4b3f93d4 35 fields · synced Jun 8, 2026