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FDA 510(k)

V-GNATHOS SUPRA

K-Number: K013769 · 2002-01-22

ApplicantMetalor Technologies USA
Decision Date2002-01-22
Product CodeEJT
Advisory CommitteeDE
DecisionSubstantially Equivalent

Device Summary

V-GNATHOS SUPRA is the device name listed in this FDA 510(k) record. The listed applicant is Metalor Technologies USA. It received FDA 510(k) clearance on 2002-01-22 under 510(k) number K013769. The device is classified under product code EJT. It was reviewed by the DE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the V-GNATHOS SUPRA?

V-GNATHOS SUPRA is a medical device that received FDA 510(k) clearance on 2002-01-22. The listed applicant is Metalor Technologies USA. The 510(k) number is K013769.

When did V-GNATHOS SUPRA receive FDA 510(k) clearance?

V-GNATHOS SUPRA received FDA 510(k) clearance on 2002-01-22, under 510(k) number K013769.

Who is the listed applicant for V-GNATHOS SUPRA?

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

What is the FDA product code for V-GNATHOS SUPRA?

The FDA product code for V-GNATHOS SUPRA is EJT.

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Other records listing Metalor Technologies USA 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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Related Devices (Code: EJT)

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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