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FDA 510(k)

ZIMMER DTO IMPLANT

K-Number: K071879 · 2007-10-05

ApplicantZimmer Spine, Inc.
Decision Date2007-10-05
Product CodeNQP
Advisory CommitteeOR
DecisionUnknown

Device Summary

ZIMMER DTO IMPLANT is the device name listed in this FDA 510(k) record. The listed applicant is Zimmer Spine, Inc.. It received FDA 510(k) clearance on 2007-10-05 under 510(k) number K071879. The device is classified under product code NQP. It was reviewed by the OR advisory panel. FDA Decision: Unknown.

Frequently Asked Questions

What is the ZIMMER DTO IMPLANT?

ZIMMER DTO IMPLANT is a medical device that received FDA 510(k) clearance on 2007-10-05. The listed applicant is Zimmer Spine, Inc.. The 510(k) number is K071879.

When did ZIMMER DTO IMPLANT receive FDA 510(k) clearance?

ZIMMER DTO IMPLANT received FDA 510(k) clearance on 2007-10-05, under 510(k) number K071879.

Who is the listed applicant for ZIMMER DTO IMPLANT?

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

What is the FDA product code for ZIMMER DTO IMPLANT?

The FDA product code for ZIMMER DTO IMPLANT is NQP.

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Other records listing Zimmer Spine, 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.

K153631Zimmer Virage OCT Spinal Fixation SystemK132790INFIX ANTERIOR LUMBAR SYSTEMK133291ST360 DEGREES SPINAL FIXATION SYSTEMK133086TITLE 2 POLYAXIAL SPINAL SYSTEMK132884PATHFINDER NXT MINIMALLY INVASIVE PEDICLE SCREW SYSTEMK131980SEQUOIA PEDICLE SCREW SYSTEM INCLUDING SPEEDLINK II TRANSVERSE CONNECTOR SYSTEM

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Related Devices (Code: NQP)

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.

K203678CD HORIZON™ Spinal SystemMedtronic Sofamor Danek USA, Inc.K191066CD Horizon™ Astute™ Spinal SystemMedtronic Sofamor Danek USA, Inc.K182928CD Horizon™ Spinal SystemMedtronic Sofamor Danek USA, Inc.K101704ZIMMER DTO PIN PRESS INSTRUMENTZimmer Spine, Inc.K101083DSS STABILIZATION SYSTEMParadigm Spine, LLCK092234DYNESYS TOP-LOADING SPINAL SYSTEMZimmer Spine, Inc.

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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