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FDA 510(k)

ZODIAC SPINAL FIXATION SYSTEM

K-Number: K050830 · 2005-06-22

Decision Date2005-06-22
Product CodeKWP
Advisory CommitteeOR
DecisionSubstantially Equivalent

Device Summary

ZODIAC SPINAL FIXATION SYSTEM is the device name listed in this FDA 510(k) record. The listed applicant is Alphatec/Nexmed. It received FDA 510(k) clearance on 2005-06-22 under 510(k) number K050830. The device is classified under product code KWP. It was reviewed by the OR advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the ZODIAC SPINAL FIXATION SYSTEM?

ZODIAC SPINAL FIXATION SYSTEM is a medical device that received FDA 510(k) clearance on 2005-06-22. The listed applicant is Alphatec/Nexmed. The 510(k) number is K050830.

When did ZODIAC SPINAL FIXATION SYSTEM receive FDA 510(k) clearance?

ZODIAC SPINAL FIXATION SYSTEM received FDA 510(k) clearance on 2005-06-22, under 510(k) number K050830.

Who is the listed applicant for ZODIAC SPINAL FIXATION SYSTEM?

The FDA 510(k) record lists Alphatec/Nexmed as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for ZODIAC SPINAL FIXATION SYSTEM?

The FDA product code for ZODIAC SPINAL FIXATION SYSTEM is KWP.

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 Alphatec/Nexmed 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.

View all 9 devices →

Related Devices (Code: KWP)

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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