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FDA 510(k)

TITANIUM VERSALOK

K-Number: K990708 · 1999-03-30

ApplicantWrightmedicaltechnologyinc
Decision Date1999-03-30
Product CodeKWP
Advisory CommitteeOR
DecisionSubstantially Equivalent

Device Summary

TITANIUM VERSALOK is the device name listed in this FDA 510(k) record. The listed applicant is Wrightmedicaltechnologyinc. It received FDA 510(k) clearance on 1999-03-30 under 510(k) number K990708. The device is classified under product code KWP. It was reviewed by the OR advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the TITANIUM VERSALOK?

TITANIUM VERSALOK is a medical device that received FDA 510(k) clearance on 1999-03-30. The listed applicant is Wrightmedicaltechnologyinc. The 510(k) number is K990708.

When did TITANIUM VERSALOK receive FDA 510(k) clearance?

TITANIUM VERSALOK received FDA 510(k) clearance on 1999-03-30, under 510(k) number K990708.

Who is the listed applicant for TITANIUM VERSALOK?

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 TITANIUM VERSALOK?

The FDA product code for TITANIUM VERSALOK is KWP.

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Related Devices (Code: KWP)

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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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