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

MODIFICATION TO: INION OTPS BIODEGRADABLE PIN

K Number: K050275 · Decision Mar 7, 2005
Classifications
1
FEI Numbers
283
Registration Numbers
283
Same Product Code
203
Applicant Total
23
Review Days
28

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Basic Information

Device Name
MODIFICATION TO: INION OTPS BIODEGRADABLE PIN
K Number
K050275
Device Class
FDA class 2
Clearance Type
Special
Regulation Number
888.3040
Medical Specialty
Orthopedic
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Inion , Ltd.
Date Received
February 7, 2005
Decision Date
March 7, 2005
Product Code
HTY
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
HTY Pin, Fixation, Smooth

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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
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
K043142 INION OTPS BIODEGRADABLE MINI PLATING SYSTEM
K031714 INION TRINION BIODEGRADABLE MENISCUS SCREW
Search all 23 clearances from Inion , Ltd. →