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FDA 510(k)

NORIAN DRILLABLE

K-Number: K073303 · 2008-07-02

ApplicantSynthes (Usa)
Decision Date2008-07-02
Product CodeOIS
Advisory CommitteeOR
DecisionUnknown

Device Summary

NORIAN DRILLABLE is the device name listed in this FDA 510(k) record. The listed applicant is Synthes (Usa). It received FDA 510(k) clearance on 2008-07-02 under 510(k) number K073303. The device is classified under product code OIS. It was reviewed by the OR advisory panel. FDA Decision: Unknown.

Frequently Asked Questions

What is the NORIAN DRILLABLE?

NORIAN DRILLABLE is a medical device that received FDA 510(k) clearance on 2008-07-02. The listed applicant is Synthes (Usa). The 510(k) number is K073303.

When did NORIAN DRILLABLE receive FDA 510(k) clearance?

NORIAN DRILLABLE received FDA 510(k) clearance on 2008-07-02, under 510(k) number K073303.

Who is the listed applicant for NORIAN DRILLABLE?

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

What is the FDA product code for NORIAN DRILLABLE?

The FDA product code for NORIAN DRILLABLE is OIS.

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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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