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

SYNTHES SCOUT VESSEL GUARD

K Number: K103558 · Decision Feb 18, 2011
Classifications
1
FEI Numbers
2
Registration Numbers
2
Same Product Code
9
Applicant Total
36
Review Days
78

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Basic Information

Device Name
SYNTHES SCOUT VESSEL GUARD
K Number
K103558
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
870.3470
Medical Specialty
Cardiovascular
Decision
Unknown
Statement or Summary
Summary
Applicant
Synthes Spine
Date Received
December 2, 2010
Decision Date
February 18, 2011
Product Code
OMR
Advisory Committee
Cardiovascular
Review Advisory Committee
CV
Third Party
N

Classifications

This FDA 510(k) entry is associated with 1 FDA classification via its product code.

Product Code Device Name
OMR Vessel Guard Or Cover

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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
K103287 SYNTHES 6.0 COCR AND CPT TI-3 RODS
K093762 SYNTHES ZERO-P
Search all 36 clearances from Synthes Spine →