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FDA 510(k)

Geistlich Bio-Gide Shape, Geistlich Bio-Gide Compressed

K-Number: K171643 · 2017-10-30

ApplicantGeistlich Pharma AG
Decision Date2017-10-30
Product CodeNPL
Advisory CommitteeDE
DecisionSubstantially Equivalent

Device Summary

Geistlich Bio-Gide Shape, Geistlich Bio-Gide Compressed is a medical device manufactured by Geistlich Pharma AG. It received FDA 510(k) clearance on 2017-10-30 under approval number K171643. 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 Bio-Gide Shape, Geistlich Bio-Gide Compressed?

Geistlich Bio-Gide Shape, Geistlich Bio-Gide Compressed is a medical device that received FDA 510(k) clearance on 2017-10-30. It is manufactured by Geistlich Pharma AG. The 510(k) number is K171643.

When was Geistlich Bio-Gide Shape, Geistlich Bio-Gide Compressed approved by the FDA?

Geistlich Bio-Gide Shape, Geistlich Bio-Gide Compressed received FDA 510(k) clearance on 2017-10-30, under approval number K171643.

What company makes Geistlich Bio-Gide Shape, Geistlich Bio-Gide Compressed?

Geistlich Bio-Gide Shape, Geistlich Bio-Gide Compressed is manufactured by Geistlich Pharma AG.

What is the FDA product code for Geistlich Bio-Gide Shape, Geistlich Bio-Gide Compressed?

The FDA product code for Geistlich Bio-Gide Shape, Geistlich Bio-Gide Compressed is 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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