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

SYNTHES SPINE PEDIATRIC ROD SYSTEM

K Number: K980761 · Decision Aug 4, 1998
Classifications
1
FEI Numbers
326
Registration Numbers
326
Same Product Code
308
Applicant Total
36
Review Days
158

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Basic Information

Device Name
SYNTHES SPINE PEDIATRIC ROD SYSTEM
K Number
K980761
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
February 27, 1998
Decision Date
August 4, 1998
Product Code
MNH
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
MNH Orthosis, Spondylolisthesis Spinal Fixation

Similar 510(k) Clearances

Other 510(k) clearances with the same product code (MNH), 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
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 →