Percuvance Percutaneous Surgical System
K-Number: K181852 · 2018-10-12
ApplicantTeleflexmedical, Inc.
Decision Date2018-10-12
Product CodeGEI
Advisory CommitteeSU
DecisionSubstantially Equivalent
Device Summary
Percuvance Percutaneous Surgical System is a medical device manufactured by Teleflexmedical, Inc.. It received FDA 510(k) clearance on 2018-10-12 under approval number K181852. The device is classified under product code GEI. It was reviewed by the SU advisory panel. FDA Decision: Substantially Equivalent.
Frequently Asked Questions
What is the Percuvance Percutaneous Surgical System?
Percuvance Percutaneous Surgical System is a medical device that received FDA 510(k) clearance on 2018-10-12. It is manufactured by Teleflexmedical, Inc.. The 510(k) number is K181852.
When was Percuvance Percutaneous Surgical System approved by the FDA?
Percuvance Percutaneous Surgical System received FDA 510(k) clearance on 2018-10-12, under approval number K181852.
What company makes Percuvance Percutaneous Surgical System?
Percuvance Percutaneous Surgical System is manufactured by Teleflexmedical, Inc..
What is the FDA product code for Percuvance Percutaneous Surgical System?
The FDA product code for Percuvance Percutaneous Surgical System is GEI.
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Official Source
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