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FDA 510(k)

NITANIUM PRO FORM ARCHWIRES,ROUND,SQUARE,RECTANGUL

K-Number: K931663 · 1993-07-08

ApplicantOrtho Organizers, Inc.
Decision Date1993-07-08
Product CodeEJF
Advisory CommitteeDE
DecisionSubstantially Equivalent

Device Summary

NITANIUM PRO FORM ARCHWIRES,ROUND,SQUARE,RECTANGUL is the device name listed in this FDA 510(k) record. The listed applicant is Ortho Organizers, Inc.. It received FDA 510(k) clearance on 1993-07-08 under 510(k) number K931663. The device is classified under product code EJF. It was reviewed by the DE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the NITANIUM PRO FORM ARCHWIRES,ROUND,SQUARE,RECTANGUL?

NITANIUM PRO FORM ARCHWIRES,ROUND,SQUARE,RECTANGUL is a medical device that received FDA 510(k) clearance on 1993-07-08. The listed applicant is Ortho Organizers, Inc.. The 510(k) number is K931663.

When did NITANIUM PRO FORM ARCHWIRES,ROUND,SQUARE,RECTANGUL receive FDA 510(k) clearance?

NITANIUM PRO FORM ARCHWIRES,ROUND,SQUARE,RECTANGUL received FDA 510(k) clearance on 1993-07-08, under 510(k) number K931663.

Who is the listed applicant for NITANIUM PRO FORM ARCHWIRES,ROUND,SQUARE,RECTANGUL?

The FDA 510(k) record lists Ortho Organizers, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for NITANIUM PRO FORM ARCHWIRES,ROUND,SQUARE,RECTANGUL?

The FDA product code for NITANIUM PRO FORM ARCHWIRES,ROUND,SQUARE,RECTANGUL is EJF.

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Other records listing Ortho Organizers, Inc. as applicant

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Related Devices (Code: EJF)

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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