FDA 510(k) FDA class 2 Substantially Equivalent 🇨🇳 China

WEGO-PTFE

K Number: K170842 · Decision Jul 31, 2017
Classifications
1
FEI Numbers
33
Registration Numbers
33
Same Product Code
16
Applicant Total
8
Review Days
132

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Basic Information

Device Name
WEGO-PTFE
K Number
K170842
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
878.5035
Medical Specialty
General, Plastic Surgery
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Foosin Medical Supplies Inc., Ltd.
Date Received
March 21, 2017
Decision Date
July 31, 2017
Product Code
NBY
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
NBY Suture, Surgical, Nonabsorbable, Expanded, Polytetraflouroethylene

Similar 510(k) Clearances

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

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Other Clearances by Foosin Medical Supplies Inc., Ltd.

K Number Device Name
K201139 WEGO-PDO Barbed Suture
K193209 Wego-Stainless Steel
K183001 WEGO-PGLA RAPID
K183004 WEGO-PGA RAPID
K142810 WEGO-PGCL Absorbable Surgical Monofilament Suture
K130735 SYNTHETIC ABSORBABLE SUTURE
K130737 SYNTHETIC ABSORBABLE SUTURE