FDA 510(k) FDA class 1 Substantially Equivalent 🇨🇭 Switzerland

OTELO LL

K Number: K151104 · Decision Jan 6, 2016
Classifications
1
FEI Numbers
656
Registration Numbers
656
Same Product Code
99
Applicant Total
44
Review Days
257

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Basic Information

Device Name
OTELO LL
K Number
K151104
Device Class
FDA class 1
Clearance Type
Traditional
Regulation Number
878.4800
Medical Specialty
General, Plastic Surgery
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Spineart
Date Received
April 24, 2015
Decision Date
January 6, 2016
Product Code
GAD
Advisory Committee
General, Plastic Surgery
Review Advisory Committee
SU
Third Party
N

Classifications

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

Product Code Device Name
GAD Retractor

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