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FDA 510(k)

INTER-OS BONE GENERATOR

K-Number: K993869 · 2000-01-19

ApplicantInter-Os Technologies, LLC
Decision Date2000-01-19
Product CodeMQN
Advisory CommitteeDE
DecisionSubstantially Equivalent

Device Summary

INTER-OS BONE GENERATOR is the device name listed in this FDA 510(k) record. The listed applicant is Inter-Os Technologies, LLC. It received FDA 510(k) clearance on 2000-01-19 under 510(k) number K993869. The device is classified under product code MQN. It was reviewed by the DE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the INTER-OS BONE GENERATOR?

INTER-OS BONE GENERATOR is a medical device that received FDA 510(k) clearance on 2000-01-19. The listed applicant is Inter-Os Technologies, LLC. The 510(k) number is K993869.

When did INTER-OS BONE GENERATOR receive FDA 510(k) clearance?

INTER-OS BONE GENERATOR received FDA 510(k) clearance on 2000-01-19, under 510(k) number K993869.

Who is the listed applicant for INTER-OS BONE GENERATOR?

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

What is the FDA product code for INTER-OS BONE GENERATOR?

The FDA product code for INTER-OS BONE GENERATOR is MQN.

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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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