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

PARADIGM INTERSPINOUS FUSION PLATE

K Number: K093438 · Decision Oct 6, 2010
Classifications
1
FEI Numbers
321
Registration Numbers
321
Same Product Code
429
Applicant Total
11
Review Days
336

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Basic Information

Device Name
PARADIGM INTERSPINOUS FUSION PLATE
K Number
K093438
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
888.3050
Medical Specialty
Orthopedic
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Paradigm Spine, LLC
Date Received
November 4, 2009
Decision Date
October 6, 2010
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

Similar 510(k) Clearances

Other 510(k) clearances with the same product code (KWP), ordered by most recent decision date.

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Other Clearances by Paradigm Spine, LLC

K Number Device Name
K153302 coflex-IF
K120491 DSS STABILIZATION SYSTEM-RIGID
K112595 COFLEX-F
K113625 DSS STABILIZATION SYSTEM
K101083 DSS STABILIZATION SYSTEM
K091944 MODIFICATION TO: DSS STABILIZATION SYSTEM
K090099 DSS STABILIZATION SYSTEM
K090408 MODIFICATION TO: DSS STABILIZATION SYSTEM
K080241 DDS STABILIZATION SYSTEM
K072969 DSS
Search all 11 clearances from Paradigm Spine, LLC →