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FDA 510(k)

OSTEONICS MICROSURFACED CDH HIP STEM

K-Number: K920250 · 1992-04-20

ApplicantStryker Corp.
Decision Date1992-04-20
Product CodeJDI
Advisory CommitteeOR
DecisionSubstantially Equivalent

Device Summary

OSTEONICS MICROSURFACED CDH HIP STEM is the device name listed in this FDA 510(k) record. The listed applicant is Stryker Corp.. It received FDA 510(k) clearance on 1992-04-20 under 510(k) number K920250. 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 OSTEONICS MICROSURFACED CDH HIP STEM?

OSTEONICS MICROSURFACED CDH HIP STEM is a medical device that received FDA 510(k) clearance on 1992-04-20. The listed applicant is Stryker Corp.. The 510(k) number is K920250.

When did OSTEONICS MICROSURFACED CDH HIP STEM receive FDA 510(k) clearance?

OSTEONICS MICROSURFACED CDH HIP STEM received FDA 510(k) clearance on 1992-04-20, under 510(k) number K920250.

Who is the listed applicant for OSTEONICS MICROSURFACED CDH HIP STEM?

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

What is the FDA product code for OSTEONICS MICROSURFACED CDH HIP STEM?

The FDA product code for OSTEONICS MICROSURFACED CDH HIP STEM is JDI.

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Other records listing Stryker 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.

K230045HipCheckK191259Stryker CrossFlow Integrated Arthroscopy PumpK182359HipCheckK122113MEMORY METAL STAPLES, EASYCLIPK122053SHAPEMATCH CUTTING GUIDEK122284HOFFMANN 3

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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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