FIXION INTRAMEDULLARY NAILING SYSTEM— 510(k) K990717
Substantially EquivalentDisco-O-Tech Medical Technologies, Ltd.
FDA 510(k) clearance K990717 for FIXION INTRAMEDULLARY NAILING SYSTEM, Substantially Equivalent on 1999-06-02. Applicant: Disco-O-Tech Medical Technologies, Ltd.. Device class: 2.
Clearance details
- Applicant
- Disco-O-Tech Medical Technologies, Ltd.
- Product code
- Code HSB
- Device class
- Class 2
- Regulation
- 21 CFR 888.3020
- Advisory panel
- Orthopedic
- Date received
- Decision date
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Location
- Washington, D.C., DC, US
Recent devices under product code HSB
view all- K261481 — Pangea Femur Reconstruction System
- K253080 — AND Medical Femoral Nail System (PFNA01); AND Medical Femoral Nail System (PFNA02)
- K261651 — Precice Max System and Precice Ankle Salvage System
- K253155 — Fule Metallic Lockable Intramedullary Nail Systems
- K253046 — HERA Interlocking Intramedullary Nailing System
More clearances from Disco-O-Tech Medical Technologies, Ltd.
view all- K032588 — MODIFICATION TO FIXION INTRAMEDULLARY NAILING SYSTEM (FIXION IM)
- K031401 — FIXION DYNAMIC HIP SCREW SYSTEM (FIXION DHS)
- K023437 — FIXION INTERLOCKING PROXIMAL FEMUR INTRAMEDULLARY NAILING SYSTEM (FIXION PF NAILING SYSTEM), FIXION INTRAMEDULLARY NAIL
- K021324 — FIXION INTRAMEDULLARY NAILING SYSTEM (FIXION IM NAILING SYSTEM)
- K012967 — MODIFICATION TO FIXION INTERLOCKING PROXIMAL FEMORAL INTRAMEDULLARY NAILING SYSTEM
Adverse events under product code HSB
product code HSB- Death
- 49
- Injury
- 12,083
- Malfunction
- 6,561
- Other
- 1
- Total
- 18,694
Source: openFDA MAUDE database, through . 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.