FDA 510(k) FDA class 2 Substantially Equivalent 🇰🇷 South Korea

GBR System

K Number: K143730 · Decision Jun 10, 2015
Classifications
1
FEI Numbers
110
Registration Numbers
110
Same Product Code
288
Applicant Total
18
Review Days
163

Basic Information

Device Name
GBR System
K Number
K143730
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
872.4760
Medical Specialty
Dental
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
JEIL MEDICAL CORPORATION
Date Received
December 29, 2014
Decision Date
June 10, 2015
Product Code
JEY
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
JEY Plate, Bone

Similar 510(k) Clearances

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Other Clearances by JEIL MEDICAL CORPORATION

K Number Device Name
K161335 Dual Top Screw System
K163308 SMARTO
K161864 ARIX Foot System
K141452 LEFORTE NEURO SYSTEM BONE PLATE AND SCREW
K132876 ARIX HAND LOCKING SYSTEM
K131566 ARIX HAND SYSTEM
K131311 ARIX FOOT SYSTEM
K112812 LEFORTE NEURO SYSTEM BONE PLATE
K101902 J TAC MODEL JT-MD-035, JT-MD-040, JT-MD-045, JT-CL-030
K103778 LEFORTE NEURO SYSTEM BONE PLATE
Search all 18 clearances from JEIL MEDICAL CORPORATION →