ZODIAC SPINAL FIXATION SYSTEM
K-Number: K050830 · 2005-06-22
Advertisement
Device Summary
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.
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.
Advertisement