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FDA 510(k)

NBD HEAD SCREW

K-Number: K050377 · 2005-04-07

ApplicantNew Business Development, LLC
Decision Date2005-04-07
Product CodeHAW
Advisory CommitteeNE
DecisionSubstantially Equivalent

Device Summary

NBD HEAD SCREW is the device name listed in this FDA 510(k) record. The listed applicant is New Business Development, LLC. It received FDA 510(k) clearance on 2005-04-07 under 510(k) number K050377. The device is classified under product code HAW. It was reviewed by the NE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the NBD HEAD SCREW?

NBD HEAD SCREW is a medical device that received FDA 510(k) clearance on 2005-04-07. The listed applicant is New Business Development, LLC. The 510(k) number is K050377.

When did NBD HEAD SCREW receive FDA 510(k) clearance?

NBD HEAD SCREW received FDA 510(k) clearance on 2005-04-07, under 510(k) number K050377.

Who is the listed applicant for NBD HEAD SCREW?

The FDA 510(k) record lists New Business Development, LLC as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for NBD HEAD SCREW?

The FDA product code for NBD HEAD SCREW is HAW.

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Other records listing New Business Development, 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.

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Related Devices (Code: HAW)

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Official Source

View on FDA Database →

Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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