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FDA 510(k)

PIONEER LATERAL PLATE SYSTEM

K-Number: K120724 · 2012-05-07

ApplicantPioneer Surgical Technology, Inc.
Decision Date2012-05-07
Product CodeKWQ
Advisory CommitteeOR
DecisionSubstantially Equivalent

Device Summary

PIONEER LATERAL PLATE SYSTEM is the device name listed in this FDA 510(k) record. The listed applicant is Pioneer Surgical Technology, Inc.. It received FDA 510(k) clearance on 2012-05-07 under 510(k) number K120724. 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 LATERAL PLATE SYSTEM?

PIONEER LATERAL PLATE SYSTEM is a medical device that received FDA 510(k) clearance on 2012-05-07. The listed applicant is Pioneer Surgical Technology, Inc.. The 510(k) number is K120724.

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

PIONEER LATERAL PLATE SYSTEM received FDA 510(k) clearance on 2012-05-07, under 510(k) number K120724.

Who is the listed applicant for PIONEER LATERAL PLATE SYSTEM?

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

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

The FDA product code for PIONEER LATERAL PLATE SYSTEM is KWQ.

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Other records listing Pioneer Surgical Technology, Inc. as applicant

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Related Devices (Code: KWQ)

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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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