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

SOLSTICE CROSS CONNECTOR

K Number: K120998 · Decision Oct 1, 2012
Classifications
1
FEI Numbers
321
Registration Numbers
321
Same Product Code
429
Applicant Total
36
Review Days
182

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Basic Information

Device Name
SOLSTICE CROSS CONNECTOR
K Number
K120998
Device Class
FDA class 2
Clearance Type
Special
Regulation Number
888.3050
Medical Specialty
Orthopedic
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Life Spine
Date Received
April 2, 2012
Decision Date
October 1, 2012
Product Code
KWP
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
KWP Appliance, Fixation, Spinal Interlaminal

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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
K111953 NAUTILUS SPINAL SYSTEM
K121116 PLATEAU SPACER SYSTEM
K113157 AILERON INTERSPINOUS FIXATION SYSTEM
Search all 36 clearances from Life Spine →