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

ULTRAPRO* HERNIA SYSTEM, MODELS UHSL, UHSM, UHSOV

K Number: K071249 · Decision Jun 5, 2007
Classifications
1
FEI Numbers
140
Registration Numbers
140
Same Product Code
332
Applicant Total
172
Review Days
32

Basic Information

Device Name
ULTRAPRO* HERNIA SYSTEM, MODELS UHSL, UHSM, UHSOV
K Number
K071249
Device Class
FDA class 2
Clearance Type
Special
Regulation Number
878.3300
Medical Specialty
General, Plastic Surgery
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
ETHICON, INC.
Date Received
May 4, 2007
Decision Date
June 5, 2007
Product Code
FTL
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
FTL Mesh, Surgical, Polymeric

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