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

ENDO GIA(TM) EXTRA LONG ADAPTER

K Number: K133762 · Decision Jan 8, 2014
Classifications
1
FEI Numbers
136
Registration Numbers
136
Same Product Code
282
Applicant Total
89
Review Days
28

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Basic Information

Device Name
ENDO GIA(TM) EXTRA LONG ADAPTER
K Number
K133762
Device Class
FDA class 2
Clearance Type
Special
Regulation Number
878.4750
Medical Specialty
General, Plastic Surgery
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Covidien, LLC
Date Received
December 11, 2013
Decision Date
January 8, 2014
Product Code
GDW
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
GDW Staple, Implantable

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