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FDA 510(k)

AUFRANC-TURNER TYPE ACETABULAR COMPON

K-Number: K813600 · 1982-01-22

ApplicantIntermedics Orthopedics
Decision Date1982-01-22
Product CodeJDI
Advisory CommitteeOR
DecisionSubstantially Equivalent

Device Summary

AUFRANC-TURNER TYPE ACETABULAR COMPON is the device name listed in this FDA 510(k) record. The listed applicant is Intermedics Orthopedics. It received FDA 510(k) clearance on 1982-01-22 under 510(k) number K813600. 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 AUFRANC-TURNER TYPE ACETABULAR COMPON?

AUFRANC-TURNER TYPE ACETABULAR COMPON is a medical device that received FDA 510(k) clearance on 1982-01-22. The listed applicant is Intermedics Orthopedics. The 510(k) number is K813600.

When did AUFRANC-TURNER TYPE ACETABULAR COMPON receive FDA 510(k) clearance?

AUFRANC-TURNER TYPE ACETABULAR COMPON received FDA 510(k) clearance on 1982-01-22, under 510(k) number K813600.

Who is the listed applicant for AUFRANC-TURNER TYPE ACETABULAR COMPON?

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

What is the FDA product code for AUFRANC-TURNER TYPE ACETABULAR COMPON?

The FDA product code for AUFRANC-TURNER TYPE ACETABULAR COMPON is JDI.

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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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