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

NEX-LINK SPINAL FIXATION SYSTEM ROD TO ROD CONNECTORS, MODELS 725, 726 SERIES

K Number: K060634 · Decision Mar 31, 2006
Classifications
1
FEI Numbers
342
Registration Numbers
342
Same Product Code
302
Applicant Total
13
Review Days
22

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Basic Information

Device Name
NEX-LINK SPINAL FIXATION SYSTEM ROD TO ROD CONNECTORS, MODELS 725, 726 SERIES
K Number
K060634
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
888.3070
Medical Specialty
Orthopedic
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Abbott Spine, Inc.
Date Received
March 9, 2006
Decision Date
March 31, 2006
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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K081622 UNIVERSAL CLAMP STAINLESS STEEL SYSTEM
K073202 ARDIS SPACER
K072672 SEQUOIA SPINAL SYSTEM, MODEL 3300 SERIES
K071174 PATHFINDER SYSTEM POLYAXIAL PEDICLE SCREWS
K062505 NEX-LINK SPINAL FIXATION SYSTEM OFFSET CONNECTORS, 2121-XX SERIES
K060009 ABBOTT SPINE UNIVERSAL CLAMP SYSTEM
K052566 NEX-LINK SPINAL FIXATION SYSTEM OPEN POLYAXIAL SCREWS, MODELS 2112, 2113, 2118, 2119, 2120. NEX-LINK SPINAL FIXATION SY
K052638 ABBOTT SPINE, INC. SPINNAKER SYSTEM
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