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FDA 510(k)

MEDTRONIC DENTAL TCP

K-Number: K092087 · 2009-12-30

Decision Date2009-12-30
Product CodeLYC
Advisory CommitteeDE
DecisionSubstantially Equivalent

Device Summary

MEDTRONIC DENTAL TCP is the device name listed in this FDA 510(k) record. The listed applicant is Medtronic Sofamor Danek USA, Inc.. It received FDA 510(k) clearance on 2009-12-30 under 510(k) number K092087. The device is classified under product code LYC. It was reviewed by the DE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the MEDTRONIC DENTAL TCP?

MEDTRONIC DENTAL TCP is a medical device that received FDA 510(k) clearance on 2009-12-30. The listed applicant is Medtronic Sofamor Danek USA, Inc.. The 510(k) number is K092087.

When did MEDTRONIC DENTAL TCP receive FDA 510(k) clearance?

MEDTRONIC DENTAL TCP received FDA 510(k) clearance on 2009-12-30, under 510(k) number K092087.

Who is the listed applicant for MEDTRONIC DENTAL TCP?

The FDA 510(k) record lists Medtronic Sofamor Danek USA, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for MEDTRONIC DENTAL TCP?

The FDA product code for MEDTRONIC DENTAL TCP is LYC.

Related Clinical Trials

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.

Other records listing Medtronic Sofamor Danek USA, Inc. 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.

View all 139 devices →

Related Devices (Code: LYC)

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.

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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