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FDA 510(k)

INTERFERENCE MEDULLARY FIT -IMF-HIP

K-Number: K831314 · 1983-07-12

ApplicantDepuy, Inc.
Decision Date1983-07-12
Product CodeJDI
Advisory CommitteeOR
DecisionSubstantially Equivalent

Device Summary

INTERFERENCE MEDULLARY FIT -IMF-HIP is the device name listed in this FDA 510(k) record. The listed applicant is Depuy, Inc.. It received FDA 510(k) clearance on 1983-07-12 under 510(k) number K831314. 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 INTERFERENCE MEDULLARY FIT -IMF-HIP?

INTERFERENCE MEDULLARY FIT -IMF-HIP is a medical device that received FDA 510(k) clearance on 1983-07-12. The listed applicant is Depuy, Inc.. The 510(k) number is K831314.

When did INTERFERENCE MEDULLARY FIT -IMF-HIP receive FDA 510(k) clearance?

INTERFERENCE MEDULLARY FIT -IMF-HIP received FDA 510(k) clearance on 1983-07-12, under 510(k) number K831314.

Who is the listed applicant for INTERFERENCE MEDULLARY FIT -IMF-HIP?

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 INTERFERENCE MEDULLARY FIT -IMF-HIP?

The FDA product code for INTERFERENCE MEDULLARY FIT -IMF-HIP is JDI.

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Related Devices (Code: JDI)

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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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