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

NobelProcera Zirconia N1 Base

K Number: K220048 · Decision Jul 29, 2022
Classifications
1
FEI Numbers
382
Registration Numbers
382
Same Product Code
708
Applicant Total
5
Review Days
204

Research this 510(k) in seconds

The Research Assistant summarizes clearance history, predicates and product-code trends — and cites every record.

Free to try · every answer cites its records

Basic Information

Device Name
NobelProcera Zirconia N1 Base
K Number
K220048
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
872.3630
Medical Specialty
Dental
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Nobel Biocare Services AG
Date Received
January 6, 2022
Decision Date
July 29, 2022
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

Similar 510(k) Clearances

Other 510(k) clearances with the same product code (NHA), ordered by most recent decision date.

View all

Other Clearances by Nobel Biocare Services AG

K Number Device Name
K231219 NobelZygoma PureSet™ Tray
K220339 Esthetic Abutments Nobel Biocare N1
K211109 N1 TiUltra TCC Implant System
K212932 Nobel Biocare NobelSpeedy Groovy / Branemark System Mk III TiUnite / Replace Select TC PureSet Tray