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

MODIFICATION TO SYNTHES USS

K Number: K000450 · Decision Mar 10, 2000
Classifications
1
FEI Numbers
354
Registration Numbers
354
Same Product Code
302
Applicant Total
36
Review Days
28

Basic Information

Device Name
MODIFICATION TO SYNTHES USS
K Number
K000450
Device Class
FDA class 2
Clearance Type
Special
Regulation Number
888.3070
Medical Specialty
Orthopedic
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
SYNTHES SPINE
Date Received
February 11, 2000
Decision Date
March 10, 2000
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

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K122211 SYNTHES NAVIGABLE PEDICLE PREPARATION INSTRUMENTS
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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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