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FDA 510(k)

ORTHOSS

K-Number: K090401 · 2010-01-08

ApplicantEd. Geistlich Soehne AG Fur Chemische Industrie
Decision Date2010-01-08
Product CodeMQV
Advisory CommitteeOR
DecisionSubstantially Equivalent

Device Summary

ORTHOSS is the device name listed in this FDA 510(k) record. The listed applicant is Ed. Geistlich Soehne AG Fur Chemische Industrie. It received FDA 510(k) clearance on 2010-01-08 under 510(k) number K090401. The device is classified under product code MQV. It was reviewed by the OR advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the ORTHOSS?

ORTHOSS is a medical device that received FDA 510(k) clearance on 2010-01-08. The listed applicant is Ed. Geistlich Soehne AG Fur Chemische Industrie. The 510(k) number is K090401.

When did ORTHOSS receive FDA 510(k) clearance?

ORTHOSS received FDA 510(k) clearance on 2010-01-08, under 510(k) number K090401.

Who is the listed applicant for ORTHOSS?

The FDA 510(k) record lists Ed. Geistlich Soehne AG Fur Chemische Industrie as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for ORTHOSS?

The FDA product code for ORTHOSS is MQV.

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Other records listing Ed. Geistlich Soehne AG Fur Chemische Industrie as applicant

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

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Official Source

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Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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