FDA 510(k) FDA class 2 Substantially Equivalent 🇮🇱 Israel

Cortex CAD/CAM Abutments

K Number: K181580 · Decision Jan 29, 2019
Classifications
1
FEI Numbers
382
Registration Numbers
382
Same Product Code
708
Applicant Total
4
Review Days
228

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
Cortex CAD/CAM Abutments
K Number
K181580
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
872.3630
Medical Specialty
Dental
Decision
Substantially Equivalent
Statement or Summary
Statement
Applicant
Cortex Dental Implants Industries , Ltd.
Date Received
June 15, 2018
Decision Date
January 29, 2019
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 Cortex Dental Implants Industries , Ltd.

K Number Device Name
K163385 Cortex Dental Implant System
K131258 SATURN DENTAL IMPLANT
K090709 CORTEX DENTAL IMPLANT SYSTEM