FDA 510(k) FDA class 2 Unknown 🇫🇮 Finland

INION SPINAL GRAFT CONTAINMENT SYSTEM

K Number: K071810 · Decision Jul 11, 2008
Classifications
1
FEI Numbers
4
Registration Numbers
4
Same Product Code
2
Applicant Total
23
Review Days
375

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Basic Information

Device Name
INION SPINAL GRAFT CONTAINMENT SYSTEM
K Number
K071810
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
888.3060
Medical Specialty
Orthopedic
Decision
Unknown
Statement or Summary
Summary
Applicant
Inion , Ltd.
Date Received
July 2, 2007
Decision Date
July 11, 2008
Product Code
OJB
Advisory Committee
Orthopedic
Review Advisory Committee
OR
Third Party
N

Classifications

This FDA 510(k) entry is associated with 1 FDA classification via its product code.

Product Code Device Name
OJB Resorbable Spinal Intervertebral Body Fixation Orthosis - Plate

Similar 510(k) Clearances

Other 510(k) clearances with the same product code (OJB), ordered by most recent decision date.

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Other Clearances by Inion , Ltd.

K Number Device Name
K063410 INION CPS/OTPS FREEDOMPLATE
K062617 MODIFICATION TO INION OTPS BIODEGRADABLE FIXATION SYSTEM
K060393 INION HEXALON BIODEGRADABLE ACL/PCL SCREW
K051821 INION S-1 BIODEGRADABLE ANTERIOR CERVICAL FUSION SYSTEM
K052624 INION OTPS BIODEGRADABLE DISTAL RADIUS PLATE
K052444 INION CPS BABY 1.5 BIOABSORBABLE FIXATION SYSTEM
K051341 INION CPS BABY 1.5 BIOABSORBABLE FIXATION SYSTEM, 40 AND 64 HOLE PLATES, MODELS PLT-1058 AND PLT-1059
K050275 MODIFICATION TO: INION OTPS BIODEGRADABLE PIN
K043142 INION OTPS BIODEGRADABLE MINI PLATING SYSTEM
K031714 INION TRINION BIODEGRADABLE MENISCUS SCREW
Search all 23 clearances from Inion , Ltd. →