ORTHOLOC 2 with 3Di Technology Pilon Fracture Plating System— 510(k) K201259

Name: FDA 510(k) clearance K201259
Creator: U.S. Food and Drug Administration
Published: 2021-01-08

Substantially Equivalent

Wrightmedicaltechnologyinc

FDA 510(k) clearance K201259 for ORTHOLOC 2 with 3Di Technology Pilon Fracture Plating System, Substantially Equivalent on 2021-01-08. Applicant: Wrightmedicaltechnologyinc. Device class: 2.

Clearance details

Applicant: Wrightmedicaltechnologyinc
Product code: Code HRS
Device class: Class 2
Regulation: 21 CFR 888.3030
Advisory panel: Orthopedic
Date received: 2020-05-11
Decision date: 2021-01-08
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Memphis, TN, US

Download summary PDF View on FDA.gov ↗

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K261647 — Tempo Plating System; Ultra Compression Screw System2026-09-03
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K262537 — Versalock Sterile Plating System2026-08-19
K260277 — MIKRON TRAUMA BONE PLATE& SCREW SYSTEM2026-08-13
K261511 — Xpert Ankle2026-07-28

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Adverse events under product code HRS

product code HRS

Death: 27
Injury: 10,340
Malfunction: 3,328
Total: 13,695

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.