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

CREODENT SOLIDEX CUSTOM ABUTMENT

K Number: K113738 · Decision Sep 17, 2013
Classifications
1
FEI Numbers
382
Registration Numbers
382
Same Product Code
708
Applicant Total
9
Review Days
637

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
CREODENT SOLIDEX CUSTOM ABUTMENT
K Number
K113738
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
872.3630
Medical Specialty
Dental
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Creodent Prosthetics, Ltd.
Date Received
December 20, 2011
Decision Date
September 17, 2013
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 Creodent Prosthetics, Ltd.

K Number Device Name
K220390 CreoDent Solidex Customized Abutment and Screw
K211427 CREOKORREKT Aligners
K202909 CreoDent Solidex Customized Abutment
K202095 CreoDent Solidex Customized Abutment and Screw
K170100 CreoDent Solidex Customized Abutment and Screw
K162734 CreoDent Solidex Customized Abutment
K160436 CreoDent Solidex Custom Abutment
K150012 CreoDent Solidex Customized Abutment