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

HARMONY PORT SYSTEM, MODEL 1907 SERIES

K Number: K050706 · Decision Apr 15, 2005
Classifications
1
FEI Numbers
80
Registration Numbers
80
Same Product Code
42
Applicant Total
33
Review Days
28

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Basic Information

Device Name
HARMONY PORT SYSTEM, MODEL 1907 SERIES
K Number
K050706
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
882.4800
Medical Specialty
Neurology
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Spinal Concepts, Inc.
Date Received
March 18, 2005
Decision Date
April 15, 2005
Product Code
GZT
Advisory Committee
Neurology
Review Advisory Committee
NE
Third Party
N

Classifications

This FDA 510(k) entry is associated with 1 FDA classification via its product code.

Product Code Device Name
GZT Retractor, Self-Retaining, For Neurosurgery

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K033517 SPINAL CONCEPTS INC. CADENCE AND TRAXIS
K031855 SPINAL CONCEPTS, INC. INSIGHT PEDICLE SCREW SYSTEM
K031985 SPINAL CONCEPTS INC. NEX-LINK SPINAL FIXATION SYSTEM
K031318 TRAXIS CEMENT RESTRICTOR
K031672 SPINAL CONCEPTS, INC. INFIX SYSTEM
K031837 MODIFICATION TO FORTITUDE CEMENT RESTRICTOR
K030087 SPINAL CONCEPTS, INC. BACFIX TI SPINAL SYSTEM
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