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

MRI Compatibility for Existing Straumann Dental Implant Systems

K Number: K190662 · Decision Jun 17, 2019
Classifications
1
FEI Numbers
324
Registration Numbers
324
Same Product Code
1545
Applicant Total
24
Review Days
94

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Basic Information

Device Name
MRI Compatibility for Existing Straumann Dental Implant Systems
K Number
K190662
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
872.3640
Medical Specialty
Dental
Decision
Substantially Equivalent
Statement or Summary
Statement
Applicant
Straumann USA, LLC
Date Received
March 15, 2019
Decision Date
June 17, 2019
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 Straumann USA, LLC

K Number Device Name
K241575 Straumann® Anatomic Healing Abutments XC (AHA)
K203753 Straumann Surgical Cassettes
K202942 Straumann 4 mm Short Implants
K192401 Straumann Screw-Retained Abutments
K171784 Straumann Dental Implant System
K162890 BLT 02.9mm SC, SLA or SLActive, RXD, Loxim, SC Closure Cap and Healing Abutments, SC Temporary Abutments, SC Variobase Abutments, SC CARES Abutment
K151590 Straumann RN Gold Abutment for Bridge
K150899 Straumann CARES Titanium Alloy (TAN) Abutment
K151324 Straumann Variobase for CEREC
K151247 NC Straumann Screw Retained Abutments
Search all 24 clearances from Straumann USA, LLC →