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FDA 510(k)

INTERPLANTA SP TOTAL HIP PROSTHESIS

K-Number: K790488 · 1979-03-28

ApplicantWaldemar Link GmbH & Co. KG
Decision Date1979-03-28
Product CodeJDI
Advisory CommitteeOR
DecisionSubstantially Equivalent

Device Summary

INTERPLANTA SP TOTAL HIP PROSTHESIS is the device name listed in this FDA 510(k) record. The listed applicant is Waldemar Link GmbH & Co. KG. It received FDA 510(k) clearance on 1979-03-28 under 510(k) number K790488. 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 INTERPLANTA SP TOTAL HIP PROSTHESIS?

INTERPLANTA SP TOTAL HIP PROSTHESIS is a medical device that received FDA 510(k) clearance on 1979-03-28. The listed applicant is Waldemar Link GmbH & Co. KG. The 510(k) number is K790488.

When did INTERPLANTA SP TOTAL HIP PROSTHESIS receive FDA 510(k) clearance?

INTERPLANTA SP TOTAL HIP PROSTHESIS received FDA 510(k) clearance on 1979-03-28, under 510(k) number K790488.

Who is the listed applicant for INTERPLANTA SP TOTAL HIP PROSTHESIS?

The FDA 510(k) record lists Waldemar Link GmbH & Co. KG as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for INTERPLANTA SP TOTAL HIP PROSTHESIS?

The FDA product code for INTERPLANTA SP TOTAL HIP PROSTHESIS 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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