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

SYNTHES SPINE ANTERIOR THORACOLUMBAR ROD CLAMP (ATRC) SYSTEM

K Number: K974525 · Decision Mar 2, 1998
Classifications
1
FEI Numbers
356
Registration Numbers
356
Same Product Code
665
Applicant Total
36
Review Days
90

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Basic Information

Device Name
SYNTHES SPINE ANTERIOR THORACOLUMBAR ROD CLAMP (ATRC) SYSTEM
K Number
K974525
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
888.3060
Medical Specialty
Orthopedic
Decision
Substantially Equivalent for Some Indications
Applicant
Synthes Spine
Date Received
December 2, 1997
Decision Date
March 2, 1998
Product Code
KWQ
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
KWQ Appliance, Fixation, Spinal Intervertebral Body

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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
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