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FDA 510(k)

PIONEER LUMBAR PLATE SYSTEM

K-Number: K090222 · 2009-04-28

Decision Date2009-04-28
Product CodeKWQ
Advisory CommitteeOR
DecisionSubstantially Equivalent

Device Summary

PIONEER LUMBAR PLATE SYSTEM is the device name listed in this FDA 510(k) record. The listed applicant is Pioneer Surgical Technology. It received FDA 510(k) clearance on 2009-04-28 under 510(k) number K090222. 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 PIONEER LUMBAR PLATE SYSTEM?

PIONEER LUMBAR PLATE SYSTEM is a medical device that received FDA 510(k) clearance on 2009-04-28. The listed applicant is Pioneer Surgical Technology. The 510(k) number is K090222.

When did PIONEER LUMBAR PLATE SYSTEM receive FDA 510(k) clearance?

PIONEER LUMBAR PLATE SYSTEM received FDA 510(k) clearance on 2009-04-28, under 510(k) number K090222.

Who is the listed applicant for PIONEER LUMBAR PLATE SYSTEM?

The FDA 510(k) record lists Pioneer Surgical Technology as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for PIONEER LUMBAR PLATE SYSTEM?

The FDA product code for PIONEER LUMBAR PLATE 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 Pioneer Surgical Technology 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.

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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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