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

SIMPLANT 18

K Number: K172239 · Decision Apr 4, 2018
Classifications
1
FEI Numbers
609
Registration Numbers
609
Same Product Code
2221
Applicant Total
52
Review Days
252

Basic Information

Device Name
SIMPLANT 18
K Number
K172239
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
892.2050
Medical Specialty
Radiology
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Dentsply Sirona
Date Received
July 26, 2017
Decision Date
April 4, 2018
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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