Ferguson Medical
FDA 510(k) & PMA Approved Devices — 57 products
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Total Devices57
Categories0
Latest FDA decision
| Type | Number | Device Name | Code | Date | Actions |
|---|---|---|---|---|---|
| 510(k) | K033153 | DICOM THEATER | LLZ | 2004-04-23 | View |
| 510(k) | K962615 | TUMORLOCALIZER MRI | MIG | 1998-03-19 | View |
| 510(k) | K963794 | PUNCTURENEEDLE | KNW | 1998-03-19 | View |
| 510(k) | K971813 | EMBLA | OLV | 1998-01-16 | View |
| 510(k) | K972217 | ORTHOPEDIC SCREW SYSTEM | HWC | 1997-11-20 | View |
| 510(k) | K972219 | ORTHOPEDIC PLATE SYSTEM | HRS | 1997-11-20 | View |
| 510(k) | K970819 | TARGOBEAM | JAK | 1997-07-14 | View |
| 510(k) | K970258 | FIXANO D.S.S. (DOUBLE SLIDING SCREWS) SYSTEM FOR OSTEOSYNTHSIS OF UNSTABLE FEMORAL NECK FRACTURES | HRS | 1997-05-22 | View |
| 510(k) | K970257 | FIXANO D.S.S. (DOUBLE SLIDING SCREWS) SYSTEM FOR OSTEOSYNTHESIS OF SUB-TROCHANTERIAN FRACTURES | HSB | 1997-05-22 | View |
| 510(k) | K970280 | FIXANO D.S.S. (DOUBLE SLIDING SCREWS) SYSTEM FOR OSTEOSYNTHESIS OF PER-TROCHANTEROAM FRACTURES | HSB | 1997-05-22 | View |
| 510(k) | K960421 | SINUSCAN 102/SINUSPRINT | LWI | 1997-04-16 | View |
| 510(k) | K963894 | SMARTGUIDE | FCG | 1997-03-11 | View |
| 510(k) | K964094 | MINIFIX | KTT | 1996-11-27 | View |
| 510(k) | K964087 | BLOCK STOP WIRES | HTY | 1996-11-25 | View |
| 510(k) | K954772 | QUICKELS QS 200 SYSTEM | DRX | 1996-07-11 | View |
| 510(k) | K954773 | QUICKELS QS 100 SYSTEM | DRX | 1996-07-11 | View |
| 510(k) | K961185 | DAUM BIOPSYNEEDLE | FCG | 1996-04-30 | View |
| 510(k) | K954756 | FIXANO I.F.O (INTERLOCKING FLEXIBLE OSTEOSYNTHESIS) SYSTEM | HSB | 1996-01-25 | View |
| 510(k) | K954757 | FIXANO D.D.S. (DOUBLE SLIDING SCREW) | HWC | 1996-01-25 | View |
| 510(k) | K931265 | FIXANO TOTAL TRAPEZIO METACARPAL PROSTHESIS, 2ND | JWI | 1995-05-22 | View |
No matching devices.
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