Biodynamic Technologies, Inc.
FDA 510(k) & PMA Approved Devices — 30 products
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Total Devices30
Categories0
Latest FDA decision
| Type | Number | Device Name | Code | Date | Actions |
|---|---|---|---|---|---|
| 510(k) | K990436 | ULTIMAX TROCHANTERIC INTRAMEDULLARY ROD SYSTEM | HSB | 1999-03-31 | View |
| 510(k) | K990481 | ULTIMAX DISTAL RADIAL (VOLAR) LOCKING PLATE SYSTEM | HRS | 1999-03-17 | View |
| 510(k) | K990513 | ULTIMAX CORTICAL BONE SCREWS | HWC | 1999-03-17 | View |
| 510(k) | K981230 | ULTIMAX DISTAL FEMORAL INTRAMEDULLARY ROD SYSTEM | HSB | 1998-06-01 | View |
| 510(k) | K980102 | BTI HUMERAL INTRAMEDULLARY ROD SYSTEM | HSB | 1998-04-03 | View |
| 510(k) | K974756 | BTI LARGE (7.0MM) CANNULATED TRANSFIXING SCREWS | HWC | 1998-03-12 | View |
| 510(k) | K972403 | BTI CORTICAL BONE SCREWS | HWC | 1997-08-29 | View |
| 510(k) | K970897 | BTI DISTAL FEMORAL INTRAMEDULLARY ROD SYSTEM | HSB | 1997-04-21 | View |
| 510(k) | K962706 | EZ-FIX CANNULATED SCREW SYSTEM | HWC | 1996-11-13 | View |
| 510(k) | K962987 | EZ-FIX SMALL CANNULATED SCREW SYSTEM | HWC | 1996-11-04 | View |
| 510(k) | K962846 | EZ-FIX COMPRESSION HIP/SUPRACONDYLAR SCREW (CHS) SYSTEM | LXT | 1996-10-23 | View |
| 510(k) | K962552 | EZ-6 PROXIMAL HUMERAL INTERAMEDULLARY ROD SYSTEM | HSB | 1996-09-25 | View |
| 510(k) | K962553 | EZ-FIX MIDSHAFT HUMERAL INTRAMEDULLARY ROD SYSTEM | HSB | 1996-08-28 | View |
| 510(k) | K954838 | EZ FIX | JEC | 1996-01-24 | View |
| 510(k) | K935593 | ANATOMIC PROPORTIONAL SHOULDER APS (HEMI-SHOULDER) SYSTEM | HSD | 1994-10-14 | View |
| 510(k) | K932918 | TOTAL KNEE KIT | HWE | 1994-09-01 | View |
| 510(k) | K926216 | BONE CEMENT RESTRICTOR | JDK | 1994-03-22 | View |
| 510(k) | K935646 | FX-CABLELOK(TM) STOP(TROCHANTER HOOK) SYSTEM | JDQ | 1994-03-09 | View |
| 510(k) | K931540 | UNIVERSAL BONE CEMENT KIT | LZN | 1994-01-27 | View |
| 510(k) | K924323 | THE UNIVERSAL BONE CEMENT RESISTOR | JDI | 1993-02-12 | View |
No matching devices.
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