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

SYNTHES USS CONNECTORS

K Number: K113149 · Decision Feb 1, 2012
Classifications
1
FEI Numbers
342
Registration Numbers
342
Same Product Code
302
Applicant Total
36
Review Days
100

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Basic Information

Device Name
SYNTHES USS CONNECTORS
K Number
K113149
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
October 24, 2011
Decision Date
February 1, 2012
Product Code
MNI
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
MNI Orthosis, Spinal Pedicle Fixation

Similar 510(k) Clearances

Other 510(k) clearances with the same product code (MNI), 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
K113044 SYNTHES MIRS
K111358 SYNTHES USS
K103558 SYNTHES SCOUT VESSEL GUARD
K103287 SYNTHES 6.0 COCR AND CPT TI-3 RODS
K093762 SYNTHES ZERO-P
Search all 36 clearances from Synthes Spine →