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

AESCULAP NEURO PATTIES

K Number: K062406 · Decision Sep 15, 2006
Classifications
1
FEI Numbers
33
Registration Numbers
33
Same Product Code
23
Applicant Total
207
Review Days
29

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Basic Information

Device Name
AESCULAP NEURO PATTIES
K Number
K062406
Device Class
FDA class 2
Clearance Type
Special
Regulation Number
882.4700
Medical Specialty
Neurology
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Aesculap, Inc.
Date Received
August 17, 2006
Decision Date
September 15, 2006
Product Code
HBA
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
HBA Neurosurgical Paddie

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K203739 ELAN 4 Electro Motor System
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