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FDA 510(k)

CONSERVE PRESSFIT FEMORAL COMPONENT

K-Number: K082673 · 2008-12-12

ApplicantWrightmedicaltechnologyinc
Decision Date2008-12-12
Product CodeKXA
Advisory CommitteeOR
DecisionSubstantially Equivalent

Device Summary

CONSERVE PRESSFIT FEMORAL COMPONENT is the device name listed in this FDA 510(k) record. The listed applicant is Wrightmedicaltechnologyinc. It received FDA 510(k) clearance on 2008-12-12 under 510(k) number K082673. The device is classified under product code KXA. It was reviewed by the OR advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the CONSERVE PRESSFIT FEMORAL COMPONENT?

CONSERVE PRESSFIT FEMORAL COMPONENT is a medical device that received FDA 510(k) clearance on 2008-12-12. The listed applicant is Wrightmedicaltechnologyinc. The 510(k) number is K082673.

When did CONSERVE PRESSFIT FEMORAL COMPONENT receive FDA 510(k) clearance?

CONSERVE PRESSFIT FEMORAL COMPONENT received FDA 510(k) clearance on 2008-12-12, under 510(k) number K082673.

Who is the listed applicant for CONSERVE PRESSFIT FEMORAL COMPONENT?

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 CONSERVE PRESSFIT FEMORAL COMPONENT?

The FDA product code for CONSERVE PRESSFIT FEMORAL COMPONENT is KXA.

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Related Devices (Code: KXA)

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

K201219Biocore9 Femoral Head Resurfacing ComponentBiocore9, LLCK092198CORMET CEMENTLESS RESURFACING FEMORAL HEADCorin USAK071053RECAP HA PRESS-FIT FEMORAL RESURFACING HEADBiomet, Inc.K070292DUROM HIP RESURFACING SYSTEM, FEMORAL COMPONENTSZimmer GmbHK062960CONSERVE FEMORAL RESURFACING COMPONENTWrightmedicaltechnologyincK043542BIOPRO TARA FEMORAL RESURFACING COMPONENTBiopro, Inc.

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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