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FDA 510(k)

ENDOSSEOUS SCREW IMPLANT

K-Number: K820163 · 1982-03-11

ApplicantGeneral A. Nitznick, D.M.D.
Decision Date1982-03-11
Product CodeDZE
Advisory CommitteeDE
DecisionSubstantially Equivalent

Device Summary

ENDOSSEOUS SCREW IMPLANT is the device name listed in this FDA 510(k) record. The listed applicant is General A. Nitznick, D.M.D.. It received FDA 510(k) clearance on 1982-03-11 under 510(k) number K820163. The device is classified under product code DZE. It was reviewed by the DE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the ENDOSSEOUS SCREW IMPLANT?

ENDOSSEOUS SCREW IMPLANT is a medical device that received FDA 510(k) clearance on 1982-03-11. The listed applicant is General A. Nitznick, D.M.D.. The 510(k) number is K820163.

When did ENDOSSEOUS SCREW IMPLANT receive FDA 510(k) clearance?

ENDOSSEOUS SCREW IMPLANT received FDA 510(k) clearance on 1982-03-11, under 510(k) number K820163.

Who is the listed applicant for ENDOSSEOUS SCREW IMPLANT?

The FDA 510(k) record lists General A. Nitznick, D.M.D. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for ENDOSSEOUS SCREW IMPLANT?

The FDA product code for ENDOSSEOUS SCREW IMPLANT is DZE.

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Related Devices (Code: DZE)

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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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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