FDA 510(k) FDA class 2 Substantially Equivalent 🇺🇸 United States

INTRAOSSEOUS FIXATION SYSTEM

K Number: K120165 · Decision Apr 17, 2012
Classifications
1
FEI Numbers
283
Registration Numbers
283
Same Product Code
203
Applicant Total
25
Review Days
89

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Basic Information

Device Name
INTRAOSSEOUS FIXATION SYSTEM
K Number
K120165
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
888.3040
Medical Specialty
Orthopedic
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Orthohelix Surgical Designs, Inc.
Date Received
January 19, 2012
Decision Date
April 17, 2012
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 Orthohelix Surgical Designs, Inc.

K Number Device Name
K141004 INTRAOSSEOUS FIXATION SYSTEM
K142148 ORTHOHELIX STAPLE SYSTEM
K141301 MAXLOCK EXTREME ELBOW FRACTURE SYSTEM
K132733 ORTHOHELIX SYNDESMOSIS FIXATION DEVICES
K132591 MAXLOCK EXTREME SYSTEM
K130832 ORTHOHELIX STAPLE SYSTEM
K131324 MAXTORQUE SCREW SYSTEM
K123203 MAXLOCK EXTREME SYSTEM MODEL MXL
K122005 MAXLOCK EXTREME SYSTEM
K121437 MINI MAXLOCK EXTREME PLATING SYSTEM
Search all 25 clearances from Orthohelix Surgical Designs, Inc. →