XP Composite
K-Number: K182780 · 2019-07-03
Decision Date2019-07-03
Product CodeEBF
Advisory CommitteeDE
DecisionSubstantially Equivalent
Device Summary
XP Composite is a medical device manufactured by S&C Polymer Silicon- Und Composite Spezialitaeten GmbH. It received FDA 510(k) clearance on 2019-07-03 under approval number K182780. The device is classified under product code EBF. It was reviewed by the DE advisory panel. FDA Decision: Substantially Equivalent.
Frequently Asked Questions
What is the XP Composite?
XP Composite is a medical device that received FDA 510(k) clearance on 2019-07-03. It is manufactured by S&C Polymer Silicon- Und Composite Spezialitaeten GmbH. The 510(k) number is K182780.
When was XP Composite approved by the FDA?
XP Composite received FDA 510(k) clearance on 2019-07-03, under approval number K182780.
What company makes XP Composite?
XP Composite is manufactured by S&C Polymer Silicon- Und Composite Spezialitaeten GmbH.
What is the FDA product code for XP Composite?
The FDA product code for XP Composite is EBF.
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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.