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FDA 510(k)

Geistlich Fibro-Gide

K-Number: K171050 · 2017-11-09

ApplicantGeistlich Pharma AG
Decision Date2017-11-09
Product CodeNPL
Advisory CommitteeDE
DecisionSubstantially Equivalent

Device Summary

Geistlich Fibro-Gide is a medical device manufactured by Geistlich Pharma AG. It received FDA 510(k) clearance on 2017-11-09 under approval number K171050. The device is classified under product code NPL. It was reviewed by the DE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the Geistlich Fibro-Gide?

Geistlich Fibro-Gide is a medical device that received FDA 510(k) clearance on 2017-11-09. It is manufactured by Geistlich Pharma AG. The 510(k) number is K171050.

When was Geistlich Fibro-Gide approved by the FDA?

Geistlich Fibro-Gide received FDA 510(k) clearance on 2017-11-09, under approval number K171050.

What company makes Geistlich Fibro-Gide?

Geistlich Fibro-Gide is manufactured by Geistlich Pharma AG.

What is the FDA product code for Geistlich Fibro-Gide?

The FDA product code for Geistlich Fibro-Gide is NPL.

Other Devices by Geistlich Pharma AG

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Related Devices (Code: NPL)

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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.

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