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FDA 510(k)

ZIMMER DTO PIN PRESS INSTRUMENT

K-Number: K101704 · 2010-08-18

ApplicantZimmer Spine, Inc.
Decision Date2010-08-18
Product CodeNQP
Advisory CommitteeOR
DecisionSubstantially Equivalent

Device Summary

ZIMMER DTO PIN PRESS INSTRUMENT 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 2010-08-18 under 510(k) number K101704. The device is classified under product code NQP. It was reviewed by the OR advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the ZIMMER DTO PIN PRESS INSTRUMENT?

ZIMMER DTO PIN PRESS INSTRUMENT is a medical device that received FDA 510(k) clearance on 2010-08-18. The listed applicant is Zimmer Spine, Inc.. The 510(k) number is K101704.

When did ZIMMER DTO PIN PRESS INSTRUMENT receive FDA 510(k) clearance?

ZIMMER DTO PIN PRESS INSTRUMENT received FDA 510(k) clearance on 2010-08-18, under 510(k) number K101704.

Who is the listed applicant for ZIMMER DTO PIN PRESS INSTRUMENT?

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 PIN PRESS INSTRUMENT?

The FDA product code for ZIMMER DTO PIN PRESS INSTRUMENT is NQP.

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Other records listing Zimmer Spine, Inc. as applicant

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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.K101083DSS STABILIZATION SYSTEMParadigm Spine, LLCK092234DYNESYS TOP-LOADING SPINAL SYSTEMZimmer Spine, Inc.K091944MODIFICATION TO: DSS STABILIZATION SYSTEMParadigm Spine, LLC

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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