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FDA 510(k)

WRIGHT PLASTER OF PARIS PELLETS

K-Number: K963562 · 1997-05-07

ApplicantWrightmedicaltechnologyinc
Decision Date1997-05-07
Product CodeMQV
Advisory CommitteeOR
DecisionSubstantially Equivalent

Device Summary

WRIGHT PLASTER OF PARIS PELLETS is the device name listed in this FDA 510(k) record. The listed applicant is Wrightmedicaltechnologyinc. It received FDA 510(k) clearance on 1997-05-07 under 510(k) number K963562. 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 WRIGHT PLASTER OF PARIS PELLETS?

WRIGHT PLASTER OF PARIS PELLETS is a medical device that received FDA 510(k) clearance on 1997-05-07. The listed applicant is Wrightmedicaltechnologyinc. The 510(k) number is K963562.

When did WRIGHT PLASTER OF PARIS PELLETS receive FDA 510(k) clearance?

WRIGHT PLASTER OF PARIS PELLETS received FDA 510(k) clearance on 1997-05-07, under 510(k) number K963562.

Who is the listed applicant for WRIGHT PLASTER OF PARIS PELLETS?

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

What is the FDA product code for WRIGHT PLASTER OF PARIS PELLETS?

The FDA product code for WRIGHT PLASTER OF PARIS PELLETS is MQV.

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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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