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FDA 510(k)

LIMA CERAMIC FEMORAL HEAD BIOLOX BY FELDMUEHLE

K-Number: K896850 · 1990-06-05

ApplicantLima Intl. Corp.
Decision Date1990-06-05
Product CodeLZO
Advisory CommitteeOR
DecisionSubstantially Equivalent

Device Summary

LIMA CERAMIC FEMORAL HEAD BIOLOX BY FELDMUEHLE is the device name listed in this FDA 510(k) record. The listed applicant is Lima Intl. Corp.. It received FDA 510(k) clearance on 1990-06-05 under 510(k) number K896850. The device is classified under product code LZO. It was reviewed by the OR advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the LIMA CERAMIC FEMORAL HEAD BIOLOX BY FELDMUEHLE?

LIMA CERAMIC FEMORAL HEAD BIOLOX BY FELDMUEHLE is a medical device that received FDA 510(k) clearance on 1990-06-05. The listed applicant is Lima Intl. Corp.. The 510(k) number is K896850.

When did LIMA CERAMIC FEMORAL HEAD BIOLOX BY FELDMUEHLE receive FDA 510(k) clearance?

LIMA CERAMIC FEMORAL HEAD BIOLOX BY FELDMUEHLE received FDA 510(k) clearance on 1990-06-05, under 510(k) number K896850.

Who is the listed applicant for LIMA CERAMIC FEMORAL HEAD BIOLOX BY FELDMUEHLE?

The FDA 510(k) record lists Lima Intl. Corp. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for LIMA CERAMIC FEMORAL HEAD BIOLOX BY FELDMUEHLE?

The FDA product code for LIMA CERAMIC FEMORAL HEAD BIOLOX BY FELDMUEHLE is LZO.

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Other records listing Lima Intl. Corp. as applicant

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.

K922613CL HIP STEM H/A COATEDK910836LIMA COLLARED CL STEMK896851PGR HIP STEM (ENDOPROSTHESIS) FOR LARGE BONE RESECK900051MOORE TYPE ENDO PROSTHESISK902621SL-SELF LOCKING TOTAL HIP-FEMORAL COMPONENTK900257MULLER TYPE ACETABULAR CUP

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Related Devices (Code: LZO)

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.

K260173M-Vizion Femoral Revision System ExtensionMedacta International S.A.K253948Momentum Acetabular Cup SystemUnited Orthopedic CorporationK261009MobileLink Acetabular Cup System – 40mm ID Inserts (various)Waldemar Link GmbH & Co. KGK260831Z1 Hip SystemZimmer, Inc.K260182Avenir® Müller Stem; Avenir Complete™ Hip SystemZimmer, Inc.K260037implantcast Packaging System UpdateImplantcast GmbH

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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