FDA 510(k) FDA class 2 Substantially Equivalent 🇮🇹 Italy

PREMIUM, SHELTA Implant Systems

K Number: K142242 · Decision Feb 2, 2015
Classifications
1
FEI Numbers
324
Registration Numbers
324
Same Product Code
1545
Applicant Total
8
Review Days
173

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Basic Information

Device Name
PREMIUM, SHELTA Implant Systems
K Number
K142242
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
872.3640
Medical Specialty
Dental
Decision
Substantially Equivalent
Statement or Summary
Statement
Applicant
Sweden & Martina S.P.A.
Date Received
August 13, 2014
Decision Date
February 2, 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

Similar 510(k) Clearances

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Other Clearances by Sweden & Martina S.P.A.

K Number Device Name
K222640 Sweden & Martina Surgical Trays
K182084 Sweden & Martina Surgical Tray (Model ZSHORTY-INT)
K180365 PRAMA White Implant Systems
K161989 PREMIUM Implant Systems SHELTA Implant Systems
K172560 PREMIUM ONE Implant Systems
K162028 PREMIUM - SHELTA Prosthetic Components
K162004 PREMIUM Implant Systems SHELTA Implant Systems