SUPERFIXATION(TM)— 510(k) K863343

Name: FDA 510(k) clearance K863343
Creator: U.S. Food and Drug Administration
Published: 1986-09-15

Substantially Equivalent

Orthopaedic Device Corp.

FDA 510(k) clearance K863343 for SUPERFIXATION(TM), Substantially Equivalent on 1986-09-15. Applicant: Orthopaedic Device Corp.. Device class: 2.

Clearance details

Applicant: Orthopaedic Device Corp.
Product code: Code KTT
Device class: Class 2
Regulation: 21 CFR 888.3030
Advisory panel: Orthopedic
Date received: 1986-08-29
Decision date: 1986-09-15
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Allendale, NJ, US

Download summary PDF View on FDA.gov ↗

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K260112 — QuikFix External Fixator: Knee-Spanning Pack2026-03-23
K253291 — Excelsior System2026-01-20
K253202 — Hoffmann LRF System2025-12-19

More clearances from Orthopaedic Device Corp.

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K870234 — P.T.H. METAL-BACKED ACETABULAR CUP1987-03-20
K862460 — FEMORAL HEMI-HIP PROSTHESIS1986-10-06
K855228 — FEMORAL HEMI-HIP PROSTHESES1986-02-11

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.