Hayes Medical, Inc.
Hayes Medical, Inc. appears in FDA public data with 0 recalls, 12 510(k) clearances, 0 FDA inspections, and 0 compliance actions on record. Its most recent 510(k) clearance was granted on January 31, 2007.
Summary
- Total Recalls
- 0
- 510(k) Clearances
- 12
- Inspections
- 0
- Compliance Actions
- 0
Recent 510(k) Clearances
| K-Number | Device | Date |
|---|---|---|
| K070061 | 36MM COCR FEMORAL HEAD AND 36MM ACETABULAR INSERT | January 31, 2007 |
| K062383 | UNISYN HA PLASMA MODULAR HIP | December 21, 2006 |
| K060635 | CONSENSUS ACETABULAR SHELL SYSTEM | April 28, 2006 |
| K030151 | CONSENSUS HIP SYSTEM, UNISYN HIP SYSTEM | April 10, 2003 |
| K030205 | CONSENSUS UNIPOLAR HEAD, COCR | April 1, 2003 |
| K021466 | CONSENSUS ACETABULAR INSERT, CROSS-LINKED POLYETHYLENE | July 24, 2002 |
| K020153 | CONSENSUS ACETABLAR SHELL, TI COATED | April 15, 2002 |
| K003649 | TRITON HIP SYSTEM | February 23, 2001 |
| K001456 | CONSENSUS KNEE SYSTEM | August 7, 2000 |
| K983004 | CONSENSUS FEMORAL COMPONENT, POROUS, COCR/TI | November 25, 1998 |
| K964395 | PATIENT SPECIFIC IMPLANT (PSI) HIP FEMORAL COMPONENT | January 27, 1997 |
| K953198 | CORTICELLOUS BONE SCREW | November 24, 1995 |