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FDA 510(k)

FIN-S MICROIMPLANT

K-Number: K120861 · 2013-02-21

ApplicantCreekside Orthodontics
Decision Date2013-02-21
Product CodeOAT
Advisory CommitteeDE
DecisionSubstantially Equivalent

Device Summary

FIN-S MICROIMPLANT is the device name listed in this FDA 510(k) record. The listed applicant is Creekside Orthodontics. It received FDA 510(k) clearance on 2013-02-21 under 510(k) number K120861. The device is classified under product code OAT. It was reviewed by the DE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the FIN-S MICROIMPLANT?

FIN-S MICROIMPLANT is a medical device that received FDA 510(k) clearance on 2013-02-21. The listed applicant is Creekside Orthodontics. The 510(k) number is K120861.

When did FIN-S MICROIMPLANT receive FDA 510(k) clearance?

FIN-S MICROIMPLANT received FDA 510(k) clearance on 2013-02-21, under 510(k) number K120861.

Who is the listed applicant for FIN-S MICROIMPLANT?

The FDA 510(k) record lists Creekside Orthodontics as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for FIN-S MICROIMPLANT?

The FDA product code for FIN-S MICROIMPLANT is OAT.

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Related Devices (Code: OAT)

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

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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