LIDGRER-LUND ACETABULAR SOCKETS— 510(k) K852369

Name: FDA 510(k) clearance K852369
Creator: U.S. Food and Drug Administration
Published: 1985-06-18

Substantially Equivalent

Link America, Inc.

FDA 510(k) clearance K852369 for LIDGRER-LUND ACETABULAR SOCKETS, Substantially Equivalent on 1985-06-18. Applicant: Link America, Inc.. Device class: 3.

Clearance details

Applicant: Link America, Inc.
Product code: Code JDL
Device class: Class 3
Regulation: 21 CFR 888.3320
Advisory panel: Orthopedic
Date received: 1985-06-04
Decision date: 1985-06-18
Decision: Substantially Equivalent
Clearance type: Traditional
Location: East Hanavor, NJ, US

Download summary PDF View on FDA.gov ↗

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K070785 — DYNASTY ACETABULAR SYSTEM2007-07-11
K061844 — DYNASTY ACETABULAR SHELL AND COCR ACETABULAR LINER2006-12-06
K051995 — PROFEMUR RENAISSANCE HIP STEM2005-08-22
K051348 — CONSERVE TOTAL FEMORAL HEAD2005-08-19

Adverse events under product code JDL

product code JDL

Injury: 285
Total: 285

Source: openFDA MAUDE database, 2020-01-01 through 2026-04-23. Counts aggregate all devices under this product code, not just this specific clearance. Reports are submissions to FDA, not validated events. Search MAUDE directly →

Data sourced from openFDA. This site is unofficial and independent of the FDA.

Clearance details

Recent devices under product code JDL

More clearances from Link America, Inc.

Adverse events under product code JDL