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FDA 510(k)

NORIAN DRILLABLE INJECT, NORIAN DRILLABLE FAST SET PUTTY

K-Number: K102722 · 2011-01-27

Decision Date2011-01-27
Product CodeMQV
Advisory CommitteeOR
DecisionSubstantially Equivalent

Device Summary

NORIAN DRILLABLE INJECT, NORIAN DRILLABLE FAST SET PUTTY is the device name listed in this FDA 510(k) record. The listed applicant is Synthes USA Products, LLC. It received FDA 510(k) clearance on 2011-01-27 under 510(k) number K102722. The device is classified under product code MQV. It was reviewed by the OR advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the NORIAN DRILLABLE INJECT, NORIAN DRILLABLE FAST SET PUTTY?

NORIAN DRILLABLE INJECT, NORIAN DRILLABLE FAST SET PUTTY is a medical device that received FDA 510(k) clearance on 2011-01-27. The listed applicant is Synthes USA Products, LLC. The 510(k) number is K102722.

When did NORIAN DRILLABLE INJECT, NORIAN DRILLABLE FAST SET PUTTY receive FDA 510(k) clearance?

NORIAN DRILLABLE INJECT, NORIAN DRILLABLE FAST SET PUTTY received FDA 510(k) clearance on 2011-01-27, under 510(k) number K102722.

Who is the listed applicant for NORIAN DRILLABLE INJECT, NORIAN DRILLABLE FAST SET PUTTY?

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

What is the FDA product code for NORIAN DRILLABLE INJECT, NORIAN DRILLABLE FAST SET PUTTY?

The FDA product code for NORIAN DRILLABLE INJECT, NORIAN DRILLABLE FAST SET PUTTY is MQV.

Related Clinical Trials

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.

Other records listing Synthes USA Products, LLC as applicant

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.

View all 45 devices →

Related Devices (Code: MQV)

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.

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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