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FDA 510(k)

CELLPLEX TCP SYNTHETIC CANCELLOUS BONE

K-Number: K031817 · 2003-07-17

ApplicantWrightmedicaltechnologyinc
Decision Date2003-07-17
Product CodeMQV
Advisory CommitteeOR
DecisionSubstantially Equivalent

Device Summary

CELLPLEX TCP SYNTHETIC CANCELLOUS BONE is the device name listed in this FDA 510(k) record. The listed applicant is Wrightmedicaltechnologyinc. It received FDA 510(k) clearance on 2003-07-17 under 510(k) number K031817. 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 CELLPLEX TCP SYNTHETIC CANCELLOUS BONE?

CELLPLEX TCP SYNTHETIC CANCELLOUS BONE is a medical device that received FDA 510(k) clearance on 2003-07-17. The listed applicant is Wrightmedicaltechnologyinc. The 510(k) number is K031817.

When did CELLPLEX TCP SYNTHETIC CANCELLOUS BONE receive FDA 510(k) clearance?

CELLPLEX TCP SYNTHETIC CANCELLOUS BONE received FDA 510(k) clearance on 2003-07-17, under 510(k) number K031817.

Who is the listed applicant for CELLPLEX TCP SYNTHETIC CANCELLOUS BONE?

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 CELLPLEX TCP SYNTHETIC CANCELLOUS BONE?

The FDA product code for CELLPLEX TCP SYNTHETIC CANCELLOUS BONE 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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