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

SYNTHES SPINE UNIVERSAL SPINAL HOOK, ROD, PEDICLE/SACRAL SCREW FIXATION SYSTEM

K Number: K980928 · Decision May 11, 1998
Classifications
1
FEI Numbers
321
Registration Numbers
321
Same Product Code
429
Applicant Total
36
Review Days
61

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Basic Information

Device Name
SYNTHES SPINE UNIVERSAL SPINAL HOOK, ROD, PEDICLE/SACRAL SCREW FIXATION SYSTEM
K Number
K980928
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
888.3050
Medical Specialty
Orthopedic
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Synthes Spine
Date Received
March 11, 1998
Decision Date
May 11, 1998
Product Code
KWP
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
KWP Appliance, Fixation, Spinal Interlaminal

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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
Search all 36 clearances from Synthes Spine →