Force Fiber Fusion Suture
K-Number: K172016 · 2017-10-03
ApplicantTeleflex Medical Incorporated
Decision Date2017-10-03
Product CodeGAT
Advisory CommitteeSU
DecisionSubstantially Equivalent
Device Summary
Force Fiber Fusion Suture is a medical device manufactured by Teleflex Medical Incorporated. It received FDA 510(k) clearance on 2017-10-03 under approval number K172016. The device is classified under product code GAT. It was reviewed by the SU advisory panel. FDA Decision: Substantially Equivalent.
Frequently Asked Questions
What is the Force Fiber Fusion Suture?
Force Fiber Fusion Suture is a medical device that received FDA 510(k) clearance on 2017-10-03. It is manufactured by Teleflex Medical Incorporated. The 510(k) number is K172016.
When was Force Fiber Fusion Suture approved by the FDA?
Force Fiber Fusion Suture received FDA 510(k) clearance on 2017-10-03, under approval number K172016.
What company makes Force Fiber Fusion Suture?
Force Fiber Fusion Suture is manufactured by Teleflex Medical Incorporated.
What is the FDA product code for Force Fiber Fusion Suture?
The FDA product code for Force Fiber Fusion Suture is GAT.
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Official Source
View on FDA Database →Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.