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

Straumann CARES Titanium Alloy (TAN) Abutment

K Number: K150899 · Decision Sep 16, 2015
Classifications
1
FEI Numbers
382
Registration Numbers
382
Same Product Code
708
Applicant Total
24
Review Days
166

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Basic Information

Device Name
Straumann CARES Titanium Alloy (TAN) Abutment
K Number
K150899
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
872.3630
Medical Specialty
Dental
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Straumann USA, LLC
Date Received
April 3, 2015
Decision Date
September 16, 2015
Product Code
NHA
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
NHA Abutment, Implant, Dental, Endosseous

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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
K151324 Straumann Variobase for CEREC
K151247 NC Straumann Screw Retained Abutments
Search all 24 clearances from Straumann USA, LLC →