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FDA 510(k)

PIONEER SURGICAL NANOSS BVF-E

K-Number: K091031 · 2009-11-17

ApplicantPioneer Surgical Technology
Decision Date2009-11-17
Product CodeMQV
Advisory CommitteeOR
DecisionSubstantially Equivalent

Device Summary

PIONEER SURGICAL NANOSS BVF-E 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 2009-11-17 under 510(k) number K091031. The device is classified under product code MQV. It was reviewed by the OR advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the PIONEER SURGICAL NANOSS BVF-E?

PIONEER SURGICAL NANOSS BVF-E is a medical device that received FDA 510(k) clearance on 2009-11-17. The listed applicant is Pioneer Surgical Technology. The 510(k) number is K091031.

When did PIONEER SURGICAL NANOSS BVF-E receive FDA 510(k) clearance?

PIONEER SURGICAL NANOSS BVF-E received FDA 510(k) clearance on 2009-11-17, under 510(k) number K091031.

Who is the listed applicant for PIONEER SURGICAL NANOSS BVF-E?

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 SURGICAL NANOSS BVF-E?

The FDA product code for PIONEER SURGICAL NANOSS BVF-E is MQV.

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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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