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

NaturalLine Abutment

K Number: K151432 · Decision Nov 5, 2015
Classifications
1
FEI Numbers
382
Registration Numbers
382
Same Product Code
708
Applicant Total
3
Review Days
161

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
NaturalLine Abutment
K Number
K151432
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
872.3630
Medical Specialty
Dental
Decision
Substantially Equivalent
Statement or Summary
Statement
Applicant
Ot Medical GmbH
Date Received
May 28, 2015
Decision Date
November 5, 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

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 Ot Medical GmbH

K Number Device Name
K151608 4plus6Line Abutment System
K113113 ENDOSSEOUS DENTAL IMPLANT