FDA 510(k) FDA unclassified Substantially Equivalent 🇺🇸 United States

NUVASIVE PERCUTANEOUS TRANSFACET/INTRAPEDICULAR SCREW

K Number: K001323 · Decision Jul 25, 2000
Classifications
1
FEI Numbers
100
Registration Numbers
100
Same Product Code
77
Applicant Total
91
Review Days
90

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Basic Information

Device Name
NUVASIVE PERCUTANEOUS TRANSFACET/INTRAPEDICULAR SCREW
K Number
K001323
Device Class
FDA unclassified
Clearance Type
Traditional
Medical Specialty
Unknown
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Nuvasive, Inc.
Date Received
April 26, 2000
Decision Date
July 25, 2000
Product Code
MRW
Advisory Committee
Unknown
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
MRW System, Facet Screw Spinal Device

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K142205 NuVasive X-CORE(R) Expandable VBR System
K141968 NUVASIVE NVM5 SYSTEM
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