Zeta Cranial Navigation System (ZNS131-US)

FDA 510(k) K242351 · Zeta Surgical, Inc.

Substantially Equivalent

510(k) numberK242351

Submission

Device name
Zeta Cranial Navigation System (ZNS131-US)
Applicant
Zeta Surgical, Inc.
Boston, MA, US
Received
August 8, 2024
Decision date
October 4, 2024
Decision
Substantially Equivalent (SESE)
Type
Special 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

Other 510(k)s with product code HAW

510(k)DeviceApplicantDecision
K253856Geniant Cranial (Navigated Neurosurgical Positioning Robot)HAW · Traditional Koh Young Technology, Inc.09/10/2026SE
K261932Leksell® Vantage Stereotactic SystemHAW · Traditional Elekta Solutions AB08/05/2026SE
K253663Zeta Navigation SystemHAW · Traditional Zeta Surgical, Inc.05/01/2026SE
K253379Stealth AXiS Cranial clinical applicationHAW · Traditional Medtronic Navigation, Inc.03/26/2026SE
K231897NeuroAlign softwareHAW · Traditional Medivis, Inc.10/21/2025SE
K251317SOLOPASS 2.0 SystemHAW · Traditional Intravent Medical Partners09/05/2025SE
K250893Ball Joint Guide Array (66295)HAW · Traditional Bayer Medical Care, Inc.09/04/2025SE
K250505Ez-FiducialsHAW · Traditional Phasor Health, LLC07/09/2025SE
K242575Stereotaxic Guiding Surgical Devices, NaoTrac SHAW · Traditional Brain Navi Biotechnology Co., Ltd.05/23/2025SE
K241327Navient Image Guide Navigation System (955-NC-NC), CranialHAW · Traditional Claronav02/05/2025SE

More from Claronav

510(k)DeviceDecision
K261471Zeta TMS Navigation SystemQFF · Special 07/09/2026SE
K253663Zeta Navigation SystemHAW · Traditional 05/01/2026SE
K251927Zeta Navigation System (ZNS131-US)SGE · Special 10/10/2025SE
K233903Zeta Cranial Navigation System (ZNS131-US)HAW · Special 01/10/2024SE
K230661Zeta Cranial Navigation SystemHAW · Traditional 09/08/2023SE

Questions and answers

When was Zeta Cranial Navigation System (ZNS131-US) cleared by the FDA?

Zeta Cranial Navigation System (ZNS131-US) (K242351) received a 510(k) decision of Substantially Equivalent on October 4, 2024, 57 days after the submission was received.

What is the product code of K242351?

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