CROSS PIN— 510(k) K961920

Name: FDA 510(k) clearance K961920
Creator: U.S. Food and Drug Administration
Published: 1996-09-17

Substantially Equivalent

Medicinelodge, Inc.

FDA 510(k) clearance K961920 for CROSS PIN, Substantially Equivalent on 1996-09-17. Applicant: Medicinelodge, Inc.. Device class: 2.

Clearance details

Applicant: Medicinelodge, Inc.
Product code: Code JDW
Device class: Class 2
Regulation: 21 CFR 888.3040
Advisory panel: Orthopedic
Date received: 1996-05-17
Decision date: 1996-09-17
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Logan, UT, US

Download summary PDF View on FDA.gov ↗

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K962705 — MLI MODULAR STAPLE1996-10-01
K961905 — MEDICINELODGE, INC. SET SCREW1996-08-06
K962194 — MLI SOFT TISSUE SCREW & WASHER SYSTEM1996-07-30

Adverse events under product code JDW

product code JDW

Injury: 717
Total: 717

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.