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

KOMPREDA

K Number: K120597 · Decision May 3, 2013
Classifications
1
FEI Numbers
100
Registration Numbers
100
Same Product Code
77
Applicant Total
12
Review Days
430

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Basic Information

Device Name
KOMPREDA
K Number
K120597
Device Class
FDA unclassified
Clearance Type
Traditional
Medical Specialty
Unknown
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Custom Spine, Inc.
Date Received
February 28, 2012
Decision Date
May 3, 2013
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

Similar 510(k) Clearances

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Other Clearances by Custom Spine, Inc.

K Number Device Name
K143143 PATHWAY ELIF
K132596 PROPOSED OPTIMUS
K111726 PATHWAY AVID
K111099 ISSYS LP SPINAL FIXATION SYSTEM
K092904 PATHWAY IVB/VBR
K091134 CUSTOM SPINE REGENT ANTERIOR CERVICAL PLATE
K090566 PATHWAY AVID
K080281 PATHWAY
K072866 ISSYS LP SPINAL FIXATION SYSTEM
K070281 ISSYS LP SPINAL FIXATION SYSTEM
Search all 12 clearances from Custom Spine, Inc. →