FDA 510(k) FDA class 2 Substantially Equivalent 🇩🇪 Germany

TROKABONE, TROKABONE STERNAL

K Number: K070179 · Decision Mar 7, 2007
Classifications
1
FEI Numbers
128
Registration Numbers
128
Same Product Code
132
Applicant Total
44
Review Days
47

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Basic Information

Device Name
TROKABONE, TROKABONE STERNAL
K Number
K070179
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
876.1075
Medical Specialty
Gastroenterology, Urology
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
PAJUNK GmbH Medizintechnologie
Date Received
January 19, 2007
Decision Date
March 7, 2007
Product Code
FCG
Advisory Committee
Gastroenterology, Urology
Review Advisory Committee
GU
Third Party
N

Classifications

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

Product Code Device Name
FCG Biopsy Needle

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K241954 SonoBlock; SonoBlock II
K230701 Stim2Go
K230201 Disposable Pre-calibrated Brain Biopsy Needle 2.0
K220897 Disposable Brain Biopsy Needle 2.0
K202699 E-Cath STIM acc. Tsui
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