FDA 510(k) FDA class 2 Substantially Equivalent 🇸🇮 Slovenia

StarWalker

K Number: K202172 · Decision Nov 19, 2020
Classifications
1
FEI Numbers
476
Registration Numbers
479
Same Product Code
2793
Applicant Total
16
Review Days
108

Basic Information

Device Name
StarWalker
K Number
K202172
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
878.4810
Medical Specialty
General, Plastic Surgery
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Fotona d.o.o.
Date Received
August 3, 2020
Decision Date
November 19, 2020
Product Code
GEX
Advisory Committee
General, Plastic Surgery
Review Advisory Committee
SU
Third Party
N

Classifications

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

Product Code Device Name
GEX Powered Laser Surgical Instrument

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Other Clearances by Fotona d.o.o.

K Number Device Name
K241785 StarFormer (M008-3T)
K242202 LightWalker Laser System Family
K234061 StarFormer
K221274 StarFormer, TightWave
K223540 AvalancheLase Family
K221712 Fotona XPulse Laser System Family (XPulse 1064 nm, XPulse 810 nm, XPulse 980 nm)
K213267 Dynamis Pro Family
K202991 Fotona XPulse Pro Laser Platform
K202985 LightWalker Laser System Family
K193656 SkyPulse
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