FDA 510(k) FDA class 2 Substantially Equivalent 🇮🇹 Italy

Assut Filbloc Permanent Sutures

K Number: K171039 · Decision Aug 29, 2017
Classifications
1
FEI Numbers
108
Registration Numbers
108
Same Product Code
84
Applicant Total
2
Review Days
145

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Basic Information

Device Name
Assut Filbloc Permanent Sutures
K Number
K171039
Device Class
FDA class 2
Clearance Type
Abbreviated
Regulation Number
878.5010
Medical Specialty
General, Plastic Surgery
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Assut Europe S.P.A.
Date Received
April 6, 2017
Decision Date
August 29, 2017
Product Code
GAW
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
GAW Suture, Nonabsorbable, Synthetic, Polypropylene

Similar 510(k) Clearances

Other 510(k) clearances with the same product code (GAW), ordered by most recent decision date.

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Other Clearances by Assut Europe S.P.A.

K Number Device Name
K021767 ASSUFIL