FDA 510(k)

DSS

K-Number: K072969 · 2008-01-24

Decision Date2008-01-24

Product CodeNQP

Advisory CommitteeOR

DecisionUnknown

Device Summary

DSS is the device name listed in this FDA 510(k) record. The listed applicant is Paradigm Spine, LLC. It received FDA 510(k) clearance on 2008-01-24 under 510(k) number K072969. 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 DSS?

DSS is a medical device that received FDA 510(k) clearance on 2008-01-24. The listed applicant is Paradigm Spine, LLC. The 510(k) number is K072969.

When did DSS receive FDA 510(k) clearance?

DSS received FDA 510(k) clearance on 2008-01-24, under 510(k) number K072969.

Who is the listed applicant for DSS?

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

What is the FDA product code for DSS?

The FDA product code for DSS is NQP.

Other records listing Paradigm Spine, 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.

K153302coflex-IF K120491DSS STABILIZATION SYSTEM-RIGID K112595COFLEX-F K113625DSS STABILIZATION SYSTEM K093438PARADIGM INTERSPINOUS FUSION PLATE K101083DSS STABILIZATION SYSTEM

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Related Devices (Code: NQP)

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, LLC K092234DYNESYS 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.