Hayes Medical, Inc.
FDA 510(k) & PMA Approved Devices — 12 products
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Total Devices12
Categories0
Latest FDA decision
| Type | Number | Device Name | Code | Date | Actions |
|---|---|---|---|---|---|
| 510(k) | K070061 | 36MM COCR FEMORAL HEAD AND 36MM ACETABULAR INSERT | LWJ | 2007-01-31 | View |
| 510(k) | K062383 | UNISYN HA PLASMA MODULAR HIP | LWJ | 2006-12-21 | View |
| 510(k) | K060635 | CONSENSUS ACETABULAR SHELL SYSTEM | LPH | 2006-04-28 | View |
| 510(k) | K030151 | CONSENSUS HIP SYSTEM, UNISYN HIP SYSTEM | LZO | 2003-04-10 | View |
| 510(k) | K030205 | CONSENSUS UNIPOLAR HEAD, COCR | KWL | 2003-04-01 | View |
| 510(k) | K021466 | CONSENSUS ACETABULAR INSERT, CROSS-LINKED POLYETHYLENE | LPH | 2002-07-24 | View |
| 510(k) | K020153 | CONSENSUS ACETABLAR SHELL, TI COATED | LPH | 2002-04-15 | View |
| 510(k) | K003649 | TRITON HIP SYSTEM | LWJ | 2001-02-23 | View |
| 510(k) | K001456 | CONSENSUS KNEE SYSTEM | JWH | 2000-08-07 | View |
| 510(k) | K983004 | CONSENSUS FEMORAL COMPONENT, POROUS, COCR/TI | JWH | 1998-11-25 | View |
| 510(k) | K964395 | PATIENT SPECIFIC IMPLANT (PSI) HIP FEMORAL COMPONENT | LZO | 1997-01-27 | View |
| 510(k) | K953198 | CORTICELLOUS BONE SCREW | HWC | 1995-11-24 | View |
No matching devices.
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