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FDA 510(k)

CEMENTLESS ZWEYMUELLER HIP ENDOPROTHES

K-Number: K822979 · 1983-01-14

ApplicantAllo Pro Corp.
Decision Date1983-01-14
Product CodeJDI
Advisory CommitteeOR
DecisionSubstantially Equivalent

Device Summary

CEMENTLESS ZWEYMUELLER HIP ENDOPROTHES is the device name listed in this FDA 510(k) record. The listed applicant is Allo Pro Corp.. It received FDA 510(k) clearance on 1983-01-14 under 510(k) number K822979. 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 CEMENTLESS ZWEYMUELLER HIP ENDOPROTHES?

CEMENTLESS ZWEYMUELLER HIP ENDOPROTHES is a medical device that received FDA 510(k) clearance on 1983-01-14. The listed applicant is Allo Pro Corp.. The 510(k) number is K822979.

When did CEMENTLESS ZWEYMUELLER HIP ENDOPROTHES receive FDA 510(k) clearance?

CEMENTLESS ZWEYMUELLER HIP ENDOPROTHES received FDA 510(k) clearance on 1983-01-14, under 510(k) number K822979.

Who is the listed applicant for CEMENTLESS ZWEYMUELLER HIP ENDOPROTHES?

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

What is the FDA product code for CEMENTLESS ZWEYMUELLER HIP ENDOPROTHES?

The FDA product code for CEMENTLESS ZWEYMUELLER HIP ENDOPROTHES is JDI.

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Other records listing Allo Pro Corp. as applicant

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Related Devices (Code: JDI)

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.

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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