FDA 510(k) FDA class 2 Substantially Equivalent 🇩🇪 Germany

DD Solid Connect® CAD/CAM Abutments (further DD Ti-Base 2CUT series)

K Number: K230218 · Decision Apr 25, 2023
Classifications
1
FEI Numbers
382
Registration Numbers
382
Same Product Code
708
Applicant Total
9
Review Days
89

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Basic Information

Device Name
DD Solid Connect® CAD/CAM Abutments (further DD Ti-Base 2CUT series)
K Number
K230218
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
872.3630
Medical Specialty
Dental
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Dental Direkt GmbH
Date Received
January 26, 2023
Decision Date
April 25, 2023
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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