FDA 510(k) FDA class 2 Substantially Equivalent 🇨🇭 Switzerland

Z5m(t)

K Number: K150021 · Decision Jul 31, 2015
Classifications
1
FEI Numbers
324
Registration Numbers
324
Same Product Code
1545
Applicant Total
9
Review Days
206

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Basic Information

Device Name
Z5m(t)
K Number
K150021
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
872.3640
Medical Specialty
Dental
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Z-Systems AG
Date Received
January 6, 2015
Decision Date
July 31, 2015
Product Code
DZE
Advisory Committee
Dental
Review Advisory Committee
DE
Third Party
N

Classifications

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

Product Code Device Name
DZE Implant, Endosseous, Root-Form

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Other Clearances by Z-Systems AG

K Number Device Name
K201878 ST-Z5
K201712 Z5-TL
K200386 Z5-BL
K190243 Z5-BL
K132881 Z5C
K131701 Z5MLB, Z5MLC
K120793 Z-LOOK3 EVO SLM
K062542 Z-LOOK3 DENTAL IMPLANT SYSTEM, MODEL Z3-XXX