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FDA 510(k)

WRIGHT PLASTER OF PARIS PELLETS (SUBJECT TO REVISION)

K-Number: K960978 · 1996-06-21

ApplicantWrightmedicaltechnologyinc
Decision Date1996-06-21
Product CodeMQV
Advisory CommitteeOR
DecisionSubstantially Equivalent

Device Summary

WRIGHT PLASTER OF PARIS PELLETS (SUBJECT TO REVISION) is the device name listed in this FDA 510(k) record. The listed applicant is Wrightmedicaltechnologyinc. It received FDA 510(k) clearance on 1996-06-21 under 510(k) number K960978. 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 (SUBJECT TO REVISION)?

WRIGHT PLASTER OF PARIS PELLETS (SUBJECT TO REVISION) is a medical device that received FDA 510(k) clearance on 1996-06-21. The listed applicant is Wrightmedicaltechnologyinc. The 510(k) number is K960978.

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

WRIGHT PLASTER OF PARIS PELLETS (SUBJECT TO REVISION) received FDA 510(k) clearance on 1996-06-21, under 510(k) number K960978.

Who is the listed applicant for WRIGHT PLASTER OF PARIS PELLETS (SUBJECT TO REVISION)?

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 (SUBJECT TO REVISION)?

The FDA product code for WRIGHT PLASTER OF PARIS PELLETS (SUBJECT TO REVISION) 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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