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FDA 510(k)

PROTRUSION CAGES

K-Number: K962007 · 1996-08-01

ApplicantDepuy, Inc.
Decision Date1996-08-01
Product CodeJDJ
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

PROTRUSION CAGES is the device name listed in this FDA 510(k) record. The listed applicant is Depuy, Inc.. It received FDA 510(k) clearance on 1996-08-01 under 510(k) number K962007. The device is classified under product code JDJ. It was reviewed by the SU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the PROTRUSION CAGES?

PROTRUSION CAGES is a medical device that received FDA 510(k) clearance on 1996-08-01. The listed applicant is Depuy, Inc.. The 510(k) number is K962007.

When did PROTRUSION CAGES receive FDA 510(k) clearance?

PROTRUSION CAGES received FDA 510(k) clearance on 1996-08-01, under 510(k) number K962007.

Who is the listed applicant for PROTRUSION CAGES?

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

What is the FDA product code for PROTRUSION CAGES?

The FDA product code for PROTRUSION CAGES is JDJ.

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Other records listing Depuy, Inc. as applicant

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Related Devices (Code: JDJ)

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.

K972760LINK, ACETABULAR REVISION MESH CUPLink America, Inc.K970957OSTEONICS RESTORATION ACETABULAR RINGOsteonics Corp.K963940EXETER MESHHowmedica, Inc.K962541REFLECTION ACETABULAR REINFORCEMENT RINGSSmith & Nephew Richards, Inc.K925883OSTEONICS MICROSTRUCTURED ACETABULAR COMPONENTSOsteonics Corp.K890450INTERMEDICS APR(TM) II FEMORAL COMPONENTIntermedics Orthopedics

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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