FDA 510(k) FDA class 2 Substantially Equivalent 🇫🇮 Finland

INION CPS ORBITAL PLATES

K Number: K122890 · Decision Jan 29, 2013
Classifications
1
FEI Numbers
106
Registration Numbers
106
Same Product Code
291
Applicant Total
14
Review Days
131

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Basic Information

Device Name
INION CPS ORBITAL PLATES
K Number
K122890
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
872.4760
Medical Specialty
Dental
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Inion OY
Date Received
September 20, 2012
Decision Date
January 29, 2013
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

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Other Clearances by Inion OY

K Number Device Name
K251441 Inion CPS 1.5 Baby Bioabsorbable Fixation System; Inion CPS 1.5/2.0/2.5 Bioabsorbable Fixation System
K251472 Inion CPS 1.5/2.0/2.5 Bioabsorbable Fixation System; Inion CPS 1.5 Baby Bioabsorbable Fixation System
K203105 Inion CompressOn Screw
K191764 Inion BioRestore
K151360 Inion Spinal Graft Containment System
K133932 INION FREEDOMPIN
K123672 INION FREEDOMSCREW (ALTERNATIVE MARKETING NAME: INION OTPS FREEDOMSCREW)
K090177 INION BIORESTORE BIODEGRADABLE BONE GRAFT SUBSTITUTE
K070998 INION BIORESTORE
K071464 INION HEXALON BIODEGRADABLE ACL/PCL SCREW
Search all 14 clearances from Inion OY →