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

INION OTPS BIODEGRADABLE DISTAL RADIUS PLATE

K Number: K052624 · Decision Nov 16, 2005
Classifications
1
FEI Numbers
519
Registration Numbers
519
Same Product Code
1313
Applicant Total
23
Review Days
54

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Basic Information

Device Name
INION OTPS BIODEGRADABLE DISTAL RADIUS PLATE
K Number
K052624
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
888.3030
Medical Specialty
Orthopedic
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Inion , Ltd.
Date Received
September 23, 2005
Decision Date
November 16, 2005
Product Code
HRS
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
HRS Plate, Fixation, Bone

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Other Clearances by Inion , Ltd.

K Number Device Name
K071810 INION SPINAL GRAFT CONTAINMENT SYSTEM
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
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. →