DYNESYS TOP-LOADING SPINAL SYSTEM
K-Number: K073347 · 2008-02-08
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Device Summary
Frequently Asked Questions
What is the DYNESYS TOP-LOADING SPINAL SYSTEM?
DYNESYS TOP-LOADING SPINAL SYSTEM is a medical device that received FDA 510(k) clearance on 2008-02-08. The listed applicant is Zimmer Spine, Inc.. The 510(k) number is K073347.
When did DYNESYS TOP-LOADING SPINAL SYSTEM receive FDA 510(k) clearance?
DYNESYS TOP-LOADING SPINAL SYSTEM received FDA 510(k) clearance on 2008-02-08, under 510(k) number K073347.
Who is the listed applicant for DYNESYS TOP-LOADING SPINAL SYSTEM?
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 DYNESYS TOP-LOADING SPINAL SYSTEM?
The FDA product code for DYNESYS TOP-LOADING SPINAL SYSTEM is NQP.
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 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.
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.
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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