FDA 510(k) FDA class 2 Unknown 🇺🇸 United States

DSS

K Number: K072969 · Decision Jan 24, 2008
Classifications
1
FEI Numbers
44
Registration Numbers
44
Same Product Code
21
Applicant Total
11
Review Days
94

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Basic Information

Device Name
DSS
K Number
K072969
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
888.3070
Medical Specialty
Orthopedic
Decision
Unknown
Statement or Summary
Summary
Applicant
Paradigm Spine, LLC
Date Received
October 22, 2007
Decision Date
January 24, 2008
Product Code
NQP
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
NQP Posterior Metal/Polymer Spinal System, Fusion

Similar 510(k) Clearances

Other 510(k) clearances with the same product code (NQP), 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
K093438 PARADIGM INTERSPINOUS FUSION PLATE
K101083 DSS STABILIZATION SYSTEM
K091944 MODIFICATION TO: DSS STABILIZATION SYSTEM
K090099 DSS STABILIZATION SYSTEM
K090408 MODIFICATION TO: DSS STABILIZATION SYSTEM
K080241 DDS STABILIZATION SYSTEM
Search all 11 clearances from Paradigm Spine, LLC →