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FDA 510(k)

FOREX CORPORATION, OPTIMA, SPINAL SYSTEM

K-Number: K020279 · 2002-06-20

ApplicantForex Corp.
Decision Date2002-06-20
Product CodeMNI
Advisory CommitteeOR
DecisionSubstantially Equivalent

Device Summary

FOREX CORPORATION, OPTIMA, SPINAL SYSTEM is the device name listed in this FDA 510(k) record. The listed applicant is Forex Corp.. It received FDA 510(k) clearance on 2002-06-20 under 510(k) number K020279. The device is classified under product code MNI. It was reviewed by the OR advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the FOREX CORPORATION, OPTIMA, SPINAL SYSTEM?

FOREX CORPORATION, OPTIMA, SPINAL SYSTEM is a medical device that received FDA 510(k) clearance on 2002-06-20. The listed applicant is Forex Corp.. The 510(k) number is K020279.

When did FOREX CORPORATION, OPTIMA, SPINAL SYSTEM receive FDA 510(k) clearance?

FOREX CORPORATION, OPTIMA, SPINAL SYSTEM received FDA 510(k) clearance on 2002-06-20, under 510(k) number K020279.

Who is the listed applicant for FOREX CORPORATION, OPTIMA, SPINAL SYSTEM?

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

What is the FDA product code for FOREX CORPORATION, OPTIMA, SPINAL SYSTEM?

The FDA product code for FOREX CORPORATION, OPTIMA, SPINAL SYSTEM is MNI.

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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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