CrossCLIP Implant System— 510(k) K142727

Name: FDA 510(k) clearance K142727
Creator: U.S. Food and Drug Administration
Published: 2014-10-24

Substantially Equivalent

Orthodiscovery Group, LLC(D.B.A. Crossroads Extremity Systems

FDA 510(k) clearance K142727 for CrossCLIP Implant System, Substantially Equivalent on 2014-10-24. Applicant: Orthodiscovery Group, LLC(D.B.A. Crossroads Extremity Systems. Device class: 2.

Clearance details

Applicant: Orthodiscovery Group, LLC(D.B.A. Crossroads Extremity Systems
Product code: Code JDR
Device class: Class 2
Regulation: 21 CFR 888.3030
Advisory panel: Orthopedic
Date received: 2014-09-23
Decision date: 2014-10-24
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Collierville, TN, US

Download summary PDF View on FDA.gov ↗

Recent devices under product code JDR

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K250712 — Linkt Compression Staple System2025-05-14
K243888 — Medline UNITE® REFLEX® Hybrid Nitinol Implant System2025-04-11
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Adverse events under product code JDR

product code JDR

Injury: 726
Malfunction: 663
Other: 1
Total: 1,390

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 →

Recalls naming K142727

K-number listed on FDA's recall record

Z-1487-2017 — MotoCLIP(TM) Super Elastic Fusion System, Size 18mm x 14mm x 14mm, REF 1442-1814, Rx Only, STERILE R.Class II·Terminated·Crossroads Extremity Systems Llc·20170216

Matched by K-number from FDA's Recall Enterprise System record (openFDA device/recallk_numbers) — these recalls explicitly list K142727.

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