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

AILERON INTERSPINOUS FIXATION SYSTEM

K Number: K113157 · Decision Mar 13, 2012
Classifications
1
FEI Numbers
342
Registration Numbers
342
Same Product Code
302
Applicant Total
36
Review Days
139

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Basic Information

Device Name
AILERON INTERSPINOUS FIXATION SYSTEM
K Number
K113157
Device Class
FDA class 2
Clearance Type
Special
Regulation Number
888.3070
Medical Specialty
Orthopedic
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Life Spine
Date Received
October 26, 2011
Decision Date
March 13, 2012
Product Code
MNI
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
MNI Orthosis, Spinal Pedicle Fixation

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Other Clearances by Life Spine

K Number Device Name
K182470 Plateau Spacer System
K160169 The Life Spine Subtalar Implant System
K150368 Tarsa-Link Wedge Fixation System
K141905 PRO-LINK WEDGE SYSTEM
K133717 LONGBOW SPACER SYSTEM
K131077 LIFE SPINE PLATEAU SPACER SYSTEM
K123373 NAUTILUS SPINAL SYSTEM
K120998 SOLSTICE CROSS CONNECTOR
K111953 NAUTILUS SPINAL SYSTEM
K121116 PLATEAU SPACER SYSTEM
Search all 36 clearances from Life Spine →