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FDA 510(k)

ADVANCED REVISION PRODUCT LINE EXTENSION

K-Number: K990030 · 1999-02-03

ApplicantWrightmedicaltechnologyinc
Decision Date1999-02-03
Product CodeJWH
Advisory CommitteeOR
DecisionSubstantially Equivalent

Device Summary

ADVANCED REVISION PRODUCT LINE EXTENSION is the device name listed in this FDA 510(k) record. The listed applicant is Wrightmedicaltechnologyinc. It received FDA 510(k) clearance on 1999-02-03 under 510(k) number K990030. 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 ADVANCED REVISION PRODUCT LINE EXTENSION?

ADVANCED REVISION PRODUCT LINE EXTENSION is a medical device that received FDA 510(k) clearance on 1999-02-03. The listed applicant is Wrightmedicaltechnologyinc. The 510(k) number is K990030.

When did ADVANCED REVISION PRODUCT LINE EXTENSION receive FDA 510(k) clearance?

ADVANCED REVISION PRODUCT LINE EXTENSION received FDA 510(k) clearance on 1999-02-03, under 510(k) number K990030.

Who is the listed applicant for ADVANCED REVISION PRODUCT LINE EXTENSION?

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 ADVANCED REVISION PRODUCT LINE EXTENSION?

The FDA product code for ADVANCED REVISION PRODUCT LINE EXTENSION 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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