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Accurian

FDA UDI

Class II (US FDA UDI)

by Medtronic Sofamor Danek, Inc.

Identity

Trade Name
Accurian FDA UDI
Generic Name
Percutaneous radio-frequency ablation system generator FDA UDI
Device Name
GENERATOR AG1000 RF GENERATOR W/STAND FDA UDI
Model / Reference
AG1000 FDA UDI
Description
GENERATOR AG1000 RF GENERATOR W/STAND FDA UDI

Identifiers

Primary DI / UDI-DI
00763000140809 FDA UDI
510(k) Number
K181864 FDA UDI
FDA Product Code
GXD FDA UDI
GMDN Term
Percutaneous radio-frequency ablation system generator FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
882.4400 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

No

FDA UDI

Serial Number

Yes

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

No

FDA UDI

Category: Percutaneous radio-frequency ablation system generator

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

Similar devices

Also classified as Percutaneous radio-frequency ablation system generator.

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 dd2fa7c0-97e0-4a4f-a6c7-97b2e858927c 36 fields · synced Jun 6, 2026