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FDA 510(k)

XIA SPINAL SYSTEM C-C ADAPTOR

K-Number: K992792 · 1999-11-16

Decision Date1999-11-16
Product CodeKWQ
Advisory CommitteeOR
DecisionSubstantially Equivalent

Device Summary

XIA SPINAL SYSTEM C-C ADAPTOR is the device name listed in this FDA 510(k) record. The listed applicant is Howmedica Osteonics Corp.. It received FDA 510(k) clearance on 1999-11-16 under 510(k) number K992792. The device is classified under product code KWQ. It was reviewed by the OR advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the XIA SPINAL SYSTEM C-C ADAPTOR?

XIA SPINAL SYSTEM C-C ADAPTOR is a medical device that received FDA 510(k) clearance on 1999-11-16. The listed applicant is Howmedica Osteonics Corp.. The 510(k) number is K992792.

When did XIA SPINAL SYSTEM C-C ADAPTOR receive FDA 510(k) clearance?

XIA SPINAL SYSTEM C-C ADAPTOR received FDA 510(k) clearance on 1999-11-16, under 510(k) number K992792.

Who is the listed applicant for XIA SPINAL SYSTEM C-C ADAPTOR?

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 C-C ADAPTOR?

The FDA product code for XIA SPINAL SYSTEM C-C ADAPTOR is KWQ.

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.

View all 288 devices →

Related Devices (Code: KWQ)

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

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Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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