Buckman Co., Inc.
FDA 510(k) & PMA Approved Devices — 111 products
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Total Devices111
Categories0
Latest FDA decision
| Type | Number | Device Name | Code | Date | Actions |
|---|---|---|---|---|---|
| 510(k) | K961320 | CROSS MEDICAL BONE PLATE SYSTEM/ CM BONE PLATE SYSTEM/CROSS TI BONE PLATE SYSTEM | HWC | 1998-06-25 | View |
| 510(k) | K974641 | FUTURELASE 3000/3002 ERBIUM LASER SYSTEM | GEX | 1998-06-08 | View |
| 510(k) | K964252 | ORTHOCHUCK | GEY | 1997-05-27 | View |
| 510(k) | K950099 | SYNERGY(TM) TI POSTERIOR SPINAL SYSTEM | MNH | 1997-01-16 | View |
| 510(k) | K960451 | WEBB-MORLEY SPINE SYSTEM | MNH | 1996-04-18 | View |
| 510(k) | K950999 | KSF POSTERIOR SPINGAL FIXATOR FOR SEVERE SPONDYLOLISTHESIS | MNH | 1996-01-25 | View |
| 510(k) | K945756 | IMAGN(TM) 2000 SYSTEM | GKZ | 1995-12-19 | View |
| 510(k) | K940003 | VOLUMET CD4 + AND CD8 + T LYMPHOCYTE COUNT TEST KIT | GKZ | 1995-10-19 | View |
| 510(k) | K951117 | LIHTAN 532 LASER | GEX | 1995-10-18 | View |
| 510(k) | K942751 | VANGUARD SERIES GAS REGULATORS | CAN | 1995-02-09 | View |
| 510(k) | K934429 | ANTERIOR SPINE SYSTEM | KWQ | 1994-10-20 | View |
| 510(k) | K931778 | LAPAROSCOPY INSTRUMENTS | GCJ | 1994-04-12 | View |
| 510(k) | K921686 | ENDOMED LAPAROSCOPY INSTRUMENTS | KNF | 1994-03-30 | View |
| 510(k) | K935950 | FX-CABLELOK CABLE/PLATE SYSTEM | JDQ | 1994-03-09 | View |
| 510(k) | K932723 | CONBIO CUB-D10 COPPER LASER SYSTEM | GEX | 1994-02-03 | View |
| 510(k) | K930634 | SUR FLO THERMAL THERAPY PADS | ILO | 1993-11-01 | View |
| 510(k) | K921056 | COTREL - DUBOUSSET SPINE IMPLANTS | KWP | 1993-06-24 | View |
| 510(k) | K921767 | COMPACT COTREL -- DUBOUSSET SPINE SYSTEM | KWP | 1993-06-22 | View |
| 510(k) | K922935 | CONBIO-MEDLITE Q-SWITCHED ND:YAG LASER SYSTEM | GEX | 1993-04-07 | View |
| 510(k) | K922919 | DYNACYT BIOPSY ASPIRATION DEVICE | MJG | 1993-03-31 | View |
No matching devices.
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