FDA 510(k) FDA class 2 Substantially Equivalent 🇺🇸 United States

Synergy Cranial v2.2.9, StealthStation Cranial v3.1.4

K Number: K221087 · Decision Jun 10, 2022
Classifications
1
FEI Numbers
250
Registration Numbers
250
Same Product Code
422
Applicant Total
35
Review Days
58

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Basic Information

Device Name
Synergy Cranial v2.2.9, StealthStation Cranial v3.1.4
K Number
K221087
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
882.4560
Medical Specialty
Neurology
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Medtronic Navigation, Inc.
Date Received
April 13, 2022
Decision Date
June 10, 2022
Product Code
HAW
Advisory Committee
Neurology
Review Advisory Committee
NE
Third Party
N

Classifications

This FDA 510(k) entry is associated with 1 FDA classification via its product code.

Product Code Device Name
HAW Neurological Stereotaxic Instrument

Similar 510(k) Clearances

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Other Clearances by Medtronic Navigation, Inc.

K Number Device Name
K253379 Stealth AXiS Cranial clinical application
K253395 Stealth AXiS™ ENT clinical application
K253391 Visualase Cooled Laser Applicator System (9735559); Visualase Cooled Laser Applicator System (9735560); Visualase Cooled Laser Applicator System (9735561)
K253381 Stealth AXiS™ Surgical System with Stealth AXiS™ Spine clinical application
K251282 StealthStation S8 Spine Software
K242464 Stealth™ Spine Clamps; ModuLeX™ Shank Mounts
K240465 O-arm O2 Imaging System
K231976 StealthStation Cranial Software, v3.1.5 (9735585)
K211269 Visualase MRI-Guided Laser Ablation System (SW 3.4)
K203639 StealthStation Cranial Software v1.3.2
Search all 35 clearances from Medtronic Navigation, Inc. →