FDA 510(k)

LIDGREN-LUND FEMORAL DYSPLASIA HIP PROSTHESIS SYS

K-Number: K852705 · 1985-08-13

Decision Date1985-08-13

Product CodeJDI

Advisory CommitteeOR

DecisionSubstantially Equivalent

Device Summary

LIDGREN-LUND FEMORAL DYSPLASIA HIP PROSTHESIS SYS 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 1985-08-13 under 510(k) number K852705. 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 LIDGREN-LUND FEMORAL DYSPLASIA HIP PROSTHESIS SYS?

LIDGREN-LUND FEMORAL DYSPLASIA HIP PROSTHESIS SYS is a medical device that received FDA 510(k) clearance on 1985-08-13. The listed applicant is Waldemar Link GmbH & Co. KG. The 510(k) number is K852705.

When did LIDGREN-LUND FEMORAL DYSPLASIA HIP PROSTHESIS SYS receive FDA 510(k) clearance?

LIDGREN-LUND FEMORAL DYSPLASIA HIP PROSTHESIS SYS received FDA 510(k) clearance on 1985-08-13, under 510(k) number K852705.

Who is the listed applicant for LIDGREN-LUND FEMORAL DYSPLASIA HIP PROSTHESIS SYS?

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 LIDGREN-LUND FEMORAL DYSPLASIA HIP PROSTHESIS SYS?

The FDA product code for LIDGREN-LUND FEMORAL DYSPLASIA HIP PROSTHESIS SYS is JDI.

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Official Source

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Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.