Disc-O-Tech Medical Technologies, Ltd.
Disc-O-Tech Medical Technologies, Ltd. holds FDA 510(k) medical device clearances, first cleared 2001, most recent 2007.
Top product codes for Disc-O-Tech Medical Technologies, Ltd.
Recent clearances by Disc-O-Tech Medical Technologies, Ltd.
- K071375 — MESH FENESTRATED INTRODUCER NEEDLE (MESH INTRODUCER NEEDLE)
- K071679 — METAFIX AND FIXION FA INTRAMEDULLARY NAILING SYSTEMS
- K063067 — CONFIDENCE FENESTRATED INTRODUCER NEEDLE
- K062424 — CONFIDENCE EX HIGH VISCOSITY BONE CEMENT
- K060300 — CONFIDENCE HIGH VISCOSITY BONE CEMENT
- K040612 — SKY BONE EXPANDER SYSTEM (SKY SYSTEM)
- K040939 — SKY BONE EXPANDER SYSTEM (SKY SYSTEM)
- K032730 — FIXION HIP SYSTEM
- K034037 — SKY BONE EXPANDER SYSTEM
- K032358 — B-TWIN BONE EXPANDER SYSTEM (B-TWIN BE SYSTEM)
- K030972 — FIXION UNIPOLAR MODULAR HEMI-HIP SYSTEM (FIXION MH)
- K014072 — FIXION UNIPOLAR MODULAR HEMI-HIP SYSTEM (FIXION UH)
- K013449 — MODIFICATION TO FIXION INTERLOCKING INTRAMEDULLARY NAILING SYSTEM
- K010901 — FIXION INTRAMEDULLARY NAILING SYSTEM (FIXION IMN) MODEL B
- K010988 — FIXION INTERLOCKING PROXIMAL FEMORAL NAILING SYSTEM
- K011390 — BONUS-ORTHOPEDIC BONE SCREW FIXATION SYSTEM
Data sourced from openFDA. This site is unofficial and independent of the FDA.