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FDA 510(k)

ADVANCE DOUBLE HIGH INSERT

K-Number: K033890 · 2004-01-15

ApplicantWrightmedicaltechnologyinc
Decision Date2004-01-15
Product CodeJWH
Advisory CommitteeOR
DecisionSubstantially Equivalent

Device Summary

ADVANCE DOUBLE HIGH INSERT is the device name listed in this FDA 510(k) record. The listed applicant is Wrightmedicaltechnologyinc. It received FDA 510(k) clearance on 2004-01-15 under 510(k) number K033890. The device is classified under product code JWH. It was reviewed by the OR advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the ADVANCE DOUBLE HIGH INSERT?

ADVANCE DOUBLE HIGH INSERT is a medical device that received FDA 510(k) clearance on 2004-01-15. The listed applicant is Wrightmedicaltechnologyinc. The 510(k) number is K033890.

When did ADVANCE DOUBLE HIGH INSERT receive FDA 510(k) clearance?

ADVANCE DOUBLE HIGH INSERT received FDA 510(k) clearance on 2004-01-15, under 510(k) number K033890.

Who is the listed applicant for ADVANCE DOUBLE HIGH INSERT?

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 ADVANCE DOUBLE HIGH INSERT?

The FDA product code for ADVANCE DOUBLE HIGH INSERT is JWH.

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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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