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

SMALL PLATEAU SPACER SYSTEM

K Number: K093093 · Decision Oct 13, 2010
Classifications
1
FEI Numbers
339
Registration Numbers
339
Same Product Code
348
Applicant Total
36
Review Days
377

Basic Information

Device Name
SMALL PLATEAU SPACER SYSTEM
K Number
K093093
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
888.3080
Medical Specialty
Orthopedic
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Life Spine
Date Received
October 1, 2009
Decision Date
October 13, 2010
Product Code
ODP
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
ODP Intervertebral Fusion Device With Bone Graft, Cervical

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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
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