510(k) K984298

Device
Z KAT FLUROTACTIC GUIDANCE SYSTEM MKI
Applicant
Z-KAT, INC.
510(k) number
K984298
Product code
HAW  
Decision
Substantially Equivalent (SESE)
Decision date
1999-06-23
Date received
1998-12-02
Regulation
882.4560
Classification name
Neurological Stereotaxic Instrument
Medical specialty
Neurology
Review panel
Neurology
Device class
2
Clearance type
Traditional
Statement or summary
Summary
Third party reviewed
No

Applicant Contact#

Contact
RONY ABOVITZ
Address
11645 Biscayne Blvd. Suite 304 Miami FL US 33181 33181

FDA Registration Numbers#

Source Documents#

510(k) summary PDF

Other 510(k) Records For Product Code HAW  #

510(k), Device, Applicant table
510(k)DeviceApplicantDecision date
K253663Zeta Navigation SystemZeta Surgical, Inc.2026-05-01
K231897NeuroAlign softwareMedivis, Inc.2025-10-21
K251317SOLOPASS 2.0 SystemIntravent Medical Partners2025-09-05
K250893Ball Joint Guide Array (66295)Bayer Medical Care, Inc.2025-09-04
K250505EZ-FIDUCIALSPhasor Health, LLC2025-07-09
K242575Stereotaxic Guiding Surgical Devices, NaoTrac SBrain Navi Biotechnology Co., Ltd.2025-05-23
K241327Navient Image Guide Navigation System (955-NC-NC), CranialClaronav2025-02-05
K243698Alignment System Cranial, with Alignment Software Cranial with LITT; Cirq Alignment Software Cranial Biopsy; Cirq Alignment Software Cranial sEEG; VarioGuide Alignment Software Cranial; Cirq Alignment Software Cranial LITTBrainlab AG2025-01-28
K243657ClearPoint System (Software Version 3.0)ClearPoint Neuro, Inc.2025-01-24
K241333Geniant Cranial (Navigated Neurosurgical Positioning Robot)Koh Young Technology, Inc.2025-01-17
K242480FLASH EVD System (10-0002)7D Surgical ULC2024-12-27
K242351Zeta Cranial Navigation System (ZNS131-US)Zeta Surgical, Inc.2024-10-04
K233703Bone Anchor (NGS-BA-01)ClearPoint Neuro, Inc.2024-04-26
K233155ClearPointer Optical Navigation WandClearPoint Neuro, Inc.2024-01-12
K233144ClearPoint Bone Screw FiducialsClearPoint Neuro, Inc.2024-01-12

Legacy Summary#

summary

FDA Review#

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