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

The Life Spine Subtalar Implant System

K Number: K160169 · Decision Jun 23, 2016
Classifications
1
FEI Numbers
659
Registration Numbers
659
Same Product Code
1058
Applicant Total
36
Review Days
148

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Basic Information

Device Name
The Life Spine Subtalar Implant System
K Number
K160169
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
888.3040
Medical Specialty
Orthopedic
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Life Spine
Date Received
January 27, 2016
Decision Date
June 23, 2016
Product Code
HWC
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
HWC Screw, Fixation, Bone

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Other Clearances by Life Spine

K Number Device Name
K182470 Plateau Spacer 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
K113157 AILERON INTERSPINOUS FIXATION SYSTEM
Search all 36 clearances from Life Spine →