FDA 510(k) FDA class 2 Substantially Equivalent 🇦🇩 Andorra

Klockner Vega TiBase for CEREC

K Number: K170022 · Decision Nov 16, 2017
Classifications
1
FEI Numbers
382
Registration Numbers
382
Same Product Code
708
Applicant Total
11
Review Days
317

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Basic Information

Device Name
Klockner Vega TiBase for CEREC
K Number
K170022
Device Class
FDA class 2
Clearance Type
Abbreviated
Regulation Number
872.3630
Medical Specialty
Dental
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
SOADCO, S.L.
Date Received
January 3, 2017
Decision Date
November 16, 2017
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.

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Other Clearances by SOADCO, S.L.

K Number Device Name
K243128 Klockner Kits
K230103 Klockner Abutments
K173642 KLOCKNER SURGICAL BOX
K153098 KLOCKNER VEGA DENTAL IMPLANT SYSTEM
K151194 KLOCKNER DENTAL IMPLANT ABUTMENTS (II)
K122988 KLOCKNER DENTAL IMPLANT ABUTMENTS
K082200 KLOCKNER ESSENTIAL DENTAL IMPLANTS SYSTEM, MODEL ESSENTIAL CONE 1.5
K080224 KLOCKNER ESSENTIAL DENTAL IMPLANTS SYSTEM, MODELS ESSENTIAL CONE (EC), ESSENTIAL SOLID (ES) AND ECK
K052654 KLOCKNER DENTAL IMPLANT, MODEL S3M
K010132 KLOCKNER DENTAL IMPLANTS, MODELS SK, NK, IK, S3, AND S4
Search all 11 clearances from SOADCO, S.L. →