Atlas FDA

WEGO-PTFE

FDA 510(k) clearance K170842 · decided 2017-07-31

Clearance details

K-number
K170842
Device name
WEGO-PTFE
Applicant
Foosin Medical Supplies Inc., Ltd.
Decision
Substantially Equivalent
Date received
2017-03-21
Decision date
2017-07-31
Days to decision
132 days
Clearance type
Traditional
Product code
NBY
Device class
2
Regulation number
878.5035
Medical specialty
General, Plastic Surgery
Advisory committee
General, Plastic Surgery
Location
Weihai, CN
Third-party review
No
Expedited review
No

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Gazelle PTFE and Suture Delivery Device (K173335)Dura Tap, LLC2018-02-08
GOLNIT Non-Absorbable PTFE Surgical Suture (K163049)Antarma Dba Golnit Sutures2017-06-21
LS-5 ePTFE Suture (K163639)Lsi Solutions2017-06-02
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MONOTEX (K140415)Riverpoint Medical2014-03-26

Recalls involving this device

No recalls on record reference this clearance.