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

STEALTHVIZ ADVANCED PLANNING APPLICATION WITH STEALTHDTI PACKAGE

K Number: K081512 · Decision Jul 18, 2008
Classifications
1
FEI Numbers
599
Registration Numbers
599
Same Product Code
2271
Applicant Total
35
Review Days
49

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Basic Information

Device Name
STEALTHVIZ ADVANCED PLANNING APPLICATION WITH STEALTHDTI PACKAGE
K Number
K081512
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
892.2050
Medical Specialty
Radiology
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Medtronic Navigation, Inc.
Date Received
May 30, 2008
Decision Date
July 18, 2008
Product Code
LLZ
Advisory Committee
Radiology
Review Advisory Committee
RA
Third Party
N

Classifications

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

Product Code Device Name
LLZ System, Image Processing, Radiological

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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)
K221087 Synergy Cranial v2.2.9, StealthStation Cranial v3.1.4
K211269 Visualase MRI-Guided Laser Ablation System (SW 3.4)
Search all 35 clearances from Medtronic Navigation, Inc. →