OsteoMed ExtremiFix Mini & Small Cannulated Screw System— 510(k) K202680

Name: FDA 510(k) clearance K202680
Creator: U.S. Food and Drug Administration
Published: 2020-10-15

Substantially Equivalent

Osteomed, LLC

FDA 510(k) clearance K202680 for OsteoMed ExtremiFix Mini & Small Cannulated Screw System, Substantially Equivalent on 2020-10-15. Applicant: Osteomed, LLC. Device class: 2.

Clearance details

Applicant: Osteomed, LLC
Product code: Code HWC
Device class: Class 2
Regulation: 21 CFR 888.3040
Advisory panel: Orthopedic
Date received: 2020-09-15
Decision date: 2020-10-15
Decision: Substantially Equivalent
Clearance type: Special
Location: Addison, TX, US

Download summary PDF View on FDA.gov ↗

Recent devices under product code HWC

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K261057 — ActivaScrew Cannulated COM2026-09-04
K260106 — OsteoCoil GT Active Compression System2026-08-24
K262344 — Large Compression Screws2026-08-12
K253858 — GFS - Sterile Screws and Top Hat2026-08-05
K262075 — Lapidus Screw Kit2026-07-22

More clearances from Osteomed, LLC

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K212570 — OsteoPlan System2022-02-11
K202105 — OsteoMed ExtremiFix Mini & Small System Tray2020-10-29
K173391 — OsteoMed QuickFix Hybrid MMF Sterilization Tray2018-05-10
K163303 — OsteoMed ExtremiFix Mid and Large Screw System2017-04-04

Adverse events under product code HWC

product code HWC

Death: 20
Injury: 15,910
Malfunction: 8,192
Other: 1
Total: 24,123

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.