Alphatec Mfg., Inc.
FDA 510(k) & PMA Approved Devices — 20 products
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Total Devices20
Categories0
Latest FDA decision
| Type | Number | Device Name | Code | Date | Actions |
|---|---|---|---|---|---|
| 510(k) | K033090 | ICON POLYAXIAL PEDICLE SCREW SYSTEM | KWP | 2004-03-26 | View |
| 510(k) | K023299 | ALPHA MIRAGE TOP TIGHTENING SPINAL SYSTEM | MNI | 2002-12-11 | View |
| 510(k) | K020356 | ALPHA MIRAGE TOP TIGHTENING SPINAL SYSTEM | MNH | 2002-07-23 | View |
| 510(k) | K993513 | DELTALOC ANTERIOR CERVICAL PLATE SYSTEM | KWQ | 2000-04-26 | View |
| 510(k) | K993873 | ALPHATEC EXTERNAL FIXATION SYSTEM COMPRESSION/DISTRACTION ROD | KTT | 2000-01-03 | View |
| 510(k) | K992350 | PYLON INTRAMEDULLAARY NAIL SYSTEM | HSB | 1999-09-22 | View |
| 510(k) | K980788 | ALPHATEC WIRE EXTERNAL FIXATION SYSTEM | JDW | 1998-05-22 | View |
| 510(k) | K964400 | ALPHATEC EXTERNAL FIXATION SYSTEM | KTT | 1997-04-28 | View |
| 510(k) | K951846 | MIRAGE SPINAL SYSTEM FOR SEVERE SPONDYLOLISTHESIS | KWP | 1996-02-14 | View |
| 510(k) | K926417 | ALPHATEC 130-150 SLOTTED COMPRESSION HIP SCREW | KTT | 1994-09-28 | View |
| 510(k) | K930515 | ALPHA SPINAL SYSTEM | KWP | 1994-06-29 | View |
| 510(k) | K933112 | ALPHATEC COMPRESSION AND RECONSTRUCTION PLATES | HRS | 1994-02-17 | View |
| 510(k) | K925500 | ALPHATEC 130 COMPRESSION HIP SCREW | HRS | 1993-04-14 | View |
| 510(k) | K923256 | ALPHATEC 2.7 MM CANNULATED CORTICAL LAG SCREW | HWC | 1992-10-09 | View |
| 510(k) | K922167 | ALPHATEC COMPRESSION AND RECONSTRUCTION PLATES | HRS | 1992-08-06 | View |
| 510(k) | K922166 | ALPHATEC SMALL FRAGMENT SET | HWC | 1992-08-06 | View |
| 510(k) | K922322 | ALPHATEC 3.5MM ZNNULATED CORTICAL LAG SCREW | HWC | 1992-08-05 | View |
| 510(k) | K921622 | ALPHATEC COMPRESSION HIP SCREW SYSTEM | HRS | 1992-07-02 | View |
| 510(k) | K914004 | ALPHATEC CANNULATED BONE SCREWS | HWC | 1991-12-05 | View |
| 510(k) | K894959 | CYPRESS CERVICAL TRACTION EQUIPMENT, CYPRESS HALO | JEC | 1990-09-14 | View |
No matching devices.
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