XYCOR SPINAL IMPLANT
K-Number: K082466 · 2009-01-09
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Device Summary
Frequently Asked Questions
What is the XYCOR SPINAL IMPLANT?
XYCOR SPINAL IMPLANT is a medical device that received FDA 510(k) clearance on 2009-01-09. The listed applicant is Vertebration,Inc. The 510(k) number is K082466.
When did XYCOR SPINAL IMPLANT receive FDA 510(k) clearance?
XYCOR SPINAL IMPLANT received FDA 510(k) clearance on 2009-01-09, under 510(k) number K082466.
Who is the listed applicant for XYCOR SPINAL IMPLANT?
The FDA 510(k) record lists Vertebration,Inc as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for XYCOR SPINAL IMPLANT?
The FDA product code for XYCOR SPINAL IMPLANT is MQP.
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 Vertebration,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: MQP)
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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