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FDA 510(k)

INTER-OS LIMB LENGTHENER

K-Number: K031875 · 2003-10-22

ApplicantInter-Os Technologies
Decision Date2003-10-22
Product CodeKTT
Advisory CommitteeOR
DecisionSubstantially Equivalent

Device Summary

INTER-OS LIMB LENGTHENER is the device name listed in this FDA 510(k) record. The listed applicant is Inter-Os Technologies. It received FDA 510(k) clearance on 2003-10-22 under 510(k) number K031875. The device is classified under product code KTT. It was reviewed by the OR advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the INTER-OS LIMB LENGTHENER?

INTER-OS LIMB LENGTHENER is a medical device that received FDA 510(k) clearance on 2003-10-22. The listed applicant is Inter-Os Technologies. The 510(k) number is K031875.

When did INTER-OS LIMB LENGTHENER receive FDA 510(k) clearance?

INTER-OS LIMB LENGTHENER received FDA 510(k) clearance on 2003-10-22, under 510(k) number K031875.

Who is the listed applicant for INTER-OS LIMB LENGTHENER?

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

What is the FDA product code for INTER-OS LIMB LENGTHENER?

The FDA product code for INTER-OS LIMB LENGTHENER is KTT.

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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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