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FDA 510(k)

PIEZO BONE SURGERY

K-Number: K111290 · 2011-11-18

ApplicantGuilin Woodpecker Medical Instrument Co., Ltd.
Decision Date2011-11-18
Product CodeDZI
Advisory CommitteeDE
DecisionSubstantially Equivalent

Device Summary

PIEZO BONE SURGERY is the device name listed in this FDA 510(k) record. The listed applicant is Guilin Woodpecker Medical Instrument Co., Ltd.. It received FDA 510(k) clearance on 2011-11-18 under 510(k) number K111290. The device is classified under product code DZI. It was reviewed by the DE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the PIEZO BONE SURGERY?

PIEZO BONE SURGERY is a medical device that received FDA 510(k) clearance on 2011-11-18. The listed applicant is Guilin Woodpecker Medical Instrument Co., Ltd.. The 510(k) number is K111290.

When did PIEZO BONE SURGERY receive FDA 510(k) clearance?

PIEZO BONE SURGERY received FDA 510(k) clearance on 2011-11-18, under 510(k) number K111290.

Who is the listed applicant for PIEZO BONE SURGERY?

The FDA 510(k) record lists Guilin Woodpecker Medical Instrument Co., Ltd. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for PIEZO BONE SURGERY?

The FDA product code for PIEZO BONE SURGERY is DZI.

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Related Devices (Code: DZI)

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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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