EMERGE EXTERNAL FIXATION SYSTEM— 510(k) K140675

Name: FDA 510(k) clearance K140675
Creator: U.S. Food and Drug Administration
Published: 2014-06-10

Substantially Equivalent

Emerge Medical, Inc.

FDA 510(k) clearance K140675 for EMERGE EXTERNAL FIXATION SYSTEM, Substantially Equivalent on 2014-06-10. Applicant: Emerge Medical, Inc.. Device class: 2.

Clearance details

Applicant: Emerge Medical, Inc.
Product code: Code KTT
Device class: Class 2
Regulation: 21 CFR 888.3030
Advisory panel: Orthopedic
Date received: 2014-03-18
Decision date: 2014-06-10
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Denver, CO, US

Download summary PDF View on FDA.gov ↗

Recent devices under product code KTT

view all

K254087 — MAXFRAME AUTOSTRUT with Bluetooth Multi-Axial Correction System2026-06-11
K260900 — DYNEX® External Fixation Systems2026-04-17
K260112 — QuikFix External Fixator: Knee-Spanning Pack2026-03-23
K253291 — Excelsior System2026-01-20
K253202 — Hoffmann LRF System2025-12-19

Adverse events under product code KTT

product code KTT

Death: 11
Injury: 3,097
Malfunction: 1,261
Total: 4,369

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.