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FDA 510(k)

ADVANCE KNEE SYSTEM

K-Number: K972626 · 1997-09-29

ApplicantWrightmedicaltechnologyinc
Decision Date1997-09-29
Product CodeJWH
Advisory CommitteeOR
DecisionSubstantially Equivalent

Device Summary

ADVANCE KNEE SYSTEM is the device name listed in this FDA 510(k) record. The listed applicant is Wrightmedicaltechnologyinc. It received FDA 510(k) clearance on 1997-09-29 under 510(k) number K972626. 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 KNEE SYSTEM?

ADVANCE KNEE SYSTEM is a medical device that received FDA 510(k) clearance on 1997-09-29. The listed applicant is Wrightmedicaltechnologyinc. The 510(k) number is K972626.

When did ADVANCE KNEE SYSTEM receive FDA 510(k) clearance?

ADVANCE KNEE SYSTEM received FDA 510(k) clearance on 1997-09-29, under 510(k) number K972626.

Who is the listed applicant for ADVANCE KNEE SYSTEM?

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 KNEE SYSTEM?

The FDA product code for ADVANCE KNEE SYSTEM is JWH.

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Related Devices (Code: 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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