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FDA 510(k)

LINEAGE A-CLASS POLY LINER

K-Number: K052026 · 2005-12-05

ApplicantWrightmedicaltechnologyinc
Decision Date2005-12-05
Product CodeLPH
Advisory CommitteeOR
DecisionSubstantially Equivalent

Device Summary

LINEAGE A-CLASS POLY LINER is the device name listed in this FDA 510(k) record. The listed applicant is Wrightmedicaltechnologyinc. It received FDA 510(k) clearance on 2005-12-05 under 510(k) number K052026. The device is classified under product code LPH. It was reviewed by the OR advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the LINEAGE A-CLASS POLY LINER?

LINEAGE A-CLASS POLY LINER is a medical device that received FDA 510(k) clearance on 2005-12-05. The listed applicant is Wrightmedicaltechnologyinc. The 510(k) number is K052026.

When did LINEAGE A-CLASS POLY LINER receive FDA 510(k) clearance?

LINEAGE A-CLASS POLY LINER received FDA 510(k) clearance on 2005-12-05, under 510(k) number K052026.

Who is the listed applicant for LINEAGE A-CLASS POLY LINER?

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 LINEAGE A-CLASS POLY LINER?

The FDA product code for LINEAGE A-CLASS POLY LINER is LPH.

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Related Devices (Code: LPH)

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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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