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

USS ILIOSACRAL, USS POLYAXIAL

K Number: K082572 · Decision Nov 24, 2008
Classifications
1
FEI Numbers
407
Registration Numbers
407
Same Product Code
900
Applicant Total
36
Review Days
80

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Basic Information

Device Name
USS ILIOSACRAL, USS POLYAXIAL
K Number
K082572
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
888.3070
Medical Specialty
Orthopedic
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Synthes Spine
Date Received
September 5, 2008
Decision Date
November 24, 2008
Product Code
NKB
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
NKB Thoracolumbosacral Pedicle Screw System

Similar 510(k) Clearances

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

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Other Clearances by Synthes Spine

K Number Device Name
K122211 SYNTHES NAVIGABLE PEDICLE PREPARATION INSTRUMENTS
K120838 SYNTHES MATRIX SYSTEM
K111048 SYNTHES SCOUT TACK FIXATION
K120928 SYNTHES MATRIX SYSTEM
K120571 SYNTHES USS CONNECTOR
K113149 SYNTHES USS CONNECTORS
K113044 SYNTHES MIRS
K111358 SYNTHES USS
K103558 SYNTHES SCOUT VESSEL GUARD
K103287 SYNTHES 6.0 COCR AND CPT TI-3 RODS
Search all 36 clearances from Synthes Spine →