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FDA 510(k)

SYNTHES VECTRA SYSTEM

K-Number: K050451 · 2005-03-24

Decision Date2005-03-24
Product CodeKWQ
Advisory CommitteeOR
DecisionSubstantially Equivalent

Device Summary

SYNTHES VECTRA SYSTEM is the device name listed in this FDA 510(k) record. The listed applicant is Synthes Spine Co.Lp. It received FDA 510(k) clearance on 2005-03-24 under 510(k) number K050451. 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 SYNTHES VECTRA SYSTEM?

SYNTHES VECTRA SYSTEM is a medical device that received FDA 510(k) clearance on 2005-03-24. The listed applicant is Synthes Spine Co.Lp. The 510(k) number is K050451.

When did SYNTHES VECTRA SYSTEM receive FDA 510(k) clearance?

SYNTHES VECTRA SYSTEM received FDA 510(k) clearance on 2005-03-24, under 510(k) number K050451.

Who is the listed applicant for SYNTHES VECTRA SYSTEM?

The FDA 510(k) record lists Synthes Spine Co.Lp as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for SYNTHES VECTRA SYSTEM?

The FDA product code for SYNTHES VECTRA SYSTEM 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 Synthes Spine Co.Lp 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 18 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

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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