FDA 510(k) FDA unclassified Substantially Equivalent 🇺🇸 United States

LIFE SPINE FACET SCREW SPINAL SYSTEM

K Number: K090865 · Decision Jun 26, 2009
Classifications
1
FEI Numbers
100
Registration Numbers
100
Same Product Code
77
Applicant Total
36
Review Days
88

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Basic Information

Device Name
LIFE SPINE FACET SCREW SPINAL SYSTEM
K Number
K090865
Device Class
FDA unclassified
Clearance Type
Traditional
Medical Specialty
Unknown
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Life Spine
Date Received
March 30, 2009
Decision Date
June 26, 2009
Product Code
MRW
Advisory Committee
Unknown
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
MRW System, Facet Screw Spinal Device

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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 →