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FDA 510(k)

MULLER TYPE ACETABULAR CUP

K-Number: K900257 · 1990-04-18

ApplicantLima Intl. Corp.
Decision Date1990-04-18
Product CodeJDI
Advisory CommitteeOR
DecisionSubstantially Equivalent

Device Summary

MULLER TYPE ACETABULAR CUP 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 1990-04-18 under 510(k) number K900257. The device is classified under product code JDI. It was reviewed by the OR advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the MULLER TYPE ACETABULAR CUP?

MULLER TYPE ACETABULAR CUP is a medical device that received FDA 510(k) clearance on 1990-04-18. The listed applicant is Lima Intl. Corp.. The 510(k) number is K900257.

When did MULLER TYPE ACETABULAR CUP receive FDA 510(k) clearance?

MULLER TYPE ACETABULAR CUP received FDA 510(k) clearance on 1990-04-18, under 510(k) number K900257.

Who is the listed applicant for MULLER TYPE ACETABULAR CUP?

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 MULLER TYPE ACETABULAR CUP?

The FDA product code for MULLER TYPE ACETABULAR CUP is JDI.

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Other records listing Lima Intl. Corp. as applicant

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Related Devices (Code: JDI)

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K253515Zimmer Biomet OSS™ Orthopedic Salvage System OsseoTi® Sleeves and AugmentsBiomet Orthopedics, Inc.K253434OSSTM Orthopedic Salvage SystemBiomet, Inc.K243571Trabecular Metal Acetabular Revision System, Acetabular Liners and Constrained LinersZimmer BiometK240783Anthology Hip Stems; CPCS Hip Stems; Femoral Heads; R3 Acetabular Liners; Spectron Hip Stems; Synergy Hip StemsSmith & Nephew, Inc.K241716Global Modular Replacement System, Modular Replacement System, Modular Rotating Hinge Knee ComponentHowmedica Osteonics Corp., Dba Stryker OrthopaedicsK240418Stryker Orthopaedics Hip Systems Labeling UpdateHowmedica Osteonics Corp., Dba Stryker Orthopaedics

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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