XIA SPINAL SYSTEM AND XIA STAINLESS STEEL SYSTEM
K-Number: K031893 · 2003-07-17
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Device Summary
Frequently Asked Questions
What is the XIA SPINAL SYSTEM AND XIA STAINLESS STEEL SYSTEM?
XIA SPINAL SYSTEM AND XIA STAINLESS STEEL SYSTEM is a medical device that received FDA 510(k) clearance on 2003-07-17. The listed applicant is Howmedica Osteonics Corp.. The 510(k) number is K031893.
When did XIA SPINAL SYSTEM AND XIA STAINLESS STEEL SYSTEM receive FDA 510(k) clearance?
XIA SPINAL SYSTEM AND XIA STAINLESS STEEL SYSTEM received FDA 510(k) clearance on 2003-07-17, under 510(k) number K031893.
Who is the listed applicant for XIA SPINAL SYSTEM AND XIA STAINLESS STEEL SYSTEM?
The FDA 510(k) record lists Howmedica Osteonics Corp. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for XIA SPINAL SYSTEM AND XIA STAINLESS STEEL SYSTEM?
The FDA product code for XIA SPINAL SYSTEM AND XIA STAINLESS STEEL 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 Howmedica Osteonics Corp. 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.
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