Synergy Cranial v2.2.9, StealthStation Cranial v3.1.4

FDA 510(k) K221087 · Medtronic Navigation, Inc.

Substantially Equivalent

510(k) numberK221087

Submission

Device name
Synergy Cranial v2.2.9, StealthStation Cranial v3.1.4
Applicant
Medtronic Navigation, Inc.
Louisville, CO, US
Received
April 13, 2022
Decision date
June 10, 2022
Decision
Substantially Equivalent (SESE)
Type
Traditional 510(k)
Summary
510(k) summary available from FDA

Official FDA 510(k) record

Device classification

Product code
HAW – Neurological Stereotaxic Instrument
Device class
Class II (moderate risk)
Regulation
21 CFR 882.4560
Specialty
Neurology

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K242575Stereotaxic Guiding Surgical Devices, NaoTrac SHAW · Traditional Brain Navi Biotechnology Co., Ltd.05/23/2025SE
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Questions and answers

When was Synergy Cranial v2.2.9, StealthStation Cranial v3.1.4 cleared by the FDA?

Synergy Cranial v2.2.9, StealthStation Cranial v3.1.4 (K221087) received a 510(k) decision of Substantially Equivalent on June 10, 2022, 58 days after the submission was received.

What is the product code of K221087?

The FDA product code is HAW – Neurological Stereotaxic Instrument, a Class II (moderate risk) device regulated under 21 CFR 882.4560.