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FDA 510(k)

TAPERED SCREW-VENT T IMPLANT, TAPERED SCREW-VENT P IMPLANT

K-Number: K101880 · 2010-10-01

Decision Date2010-10-01
Product CodeDZE
Advisory CommitteeDE
DecisionSubstantially Equivalent

Device Summary

TAPERED SCREW-VENT T IMPLANT, TAPERED SCREW-VENT P IMPLANT is the device name listed in this FDA 510(k) record. The listed applicant is Zimmer Dental, Inc.. It received FDA 510(k) clearance on 2010-10-01 under 510(k) number K101880. 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 TAPERED SCREW-VENT T IMPLANT, TAPERED SCREW-VENT P IMPLANT?

TAPERED SCREW-VENT T IMPLANT, TAPERED SCREW-VENT P IMPLANT is a medical device that received FDA 510(k) clearance on 2010-10-01. The listed applicant is Zimmer Dental, Inc.. The 510(k) number is K101880.

When did TAPERED SCREW-VENT T IMPLANT, TAPERED SCREW-VENT P IMPLANT receive FDA 510(k) clearance?

TAPERED SCREW-VENT T IMPLANT, TAPERED SCREW-VENT P IMPLANT received FDA 510(k) clearance on 2010-10-01, under 510(k) number K101880.

Who is the listed applicant for TAPERED SCREW-VENT T IMPLANT, TAPERED SCREW-VENT P IMPLANT?

The FDA 510(k) record lists Zimmer Dental, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for TAPERED SCREW-VENT T IMPLANT, TAPERED SCREW-VENT P IMPLANT?

The FDA product code for TAPERED SCREW-VENT T IMPLANT, TAPERED SCREW-VENT P IMPLANT is DZE.

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 Zimmer Dental, Inc. 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: 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.

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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