Kinamed, Inc.
FDA 510(k) & PMA Approved Devices — 33 products
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Total Devices33
Categories0
Latest FDA decision
| Type | Number | Device Name | Code | Date | Actions |
|---|---|---|---|---|---|
| 510(k) | K122049 | NEUROPRO LOW PROFILE CRANIAL PLATING SYSTEM | GWO | 2013-04-05 | View |
| 510(k) | K072250 | SUPERCABLE GRIP AND PLATE SYSTEM | KTT | 2007-11-09 | View |
| 510(k) | K050897 | NAVIPRO SHOULDER SOFTWARE MODULE | HAW | 2005-05-24 | View |
| 510(k) | K033668 | NAVIPRO KNEE SOFTWARE MODULE | HAW | 2004-03-11 | View |
| 510(k) | K032950 | GEM INSET PATELLAR COMPONENT | JWH | 2003-12-19 | View |
| 510(k) | K030256 | ISO-ELASTIC CERCLAGE SYSTEM | JDQ | 2003-10-21 | View |
| 510(k) | K020764 | NAVIPRO | HAW | 2002-06-03 | View |
| 510(k) | K013982 | KINEMATCH PATELLO-FEMORAL RESURFACING IMPALANT | KRR | 2002-05-21 | View |
| 510(k) | K010101 | GEM POSTERIOR STABILIZED TOTAL KNEE SYSTEM | JWH | 2001-05-17 | View |
| 510(k) | K003347 | ORTHOPILOT | HAW | 2001-02-23 | View |
| 510(k) | K994214 | GEM KNEE SYSTEM | JWH | 2000-07-19 | View |
| 510(k) | K982927 | QUICK TAP SELF DRILLING SCREW | DZL | 1998-09-08 | View |
| 510(k) | K964362 | KINAMED PROFIX SYSTEM | HRS | 1997-01-16 | View |
| 510(k) | K954219 | REALITY LONG STEM HIP SYSTEM | JDI | 1995-12-04 | View |
| 510(k) | K954213 | ATH FULL PROFILE ACETABULAR CUP SYSTEM | LPH | 1995-10-25 | View |
| 510(k) | K922247 | KINAMED REALITY TOTAL HIP SYSTEM | LZO | 1994-03-30 | View |
| 510(k) | K920290 | KINAMED 32MM BIOCERAM-Z TOATAL HIP FEMORAL BALL | LZO | 1992-11-03 | View |
| 510(k) | K920219 | KINAMED 26MM BIOCERAN-Z TOTAL HIP FEMORAL BALL | LZO | 1992-10-30 | View |
| 510(k) | K922421 | KINAMED ATH-POROUS AND ATH-POROUS LONG TOTAL HIP | JDI | 1992-10-15 | View |
| 510(k) | K915310 | KINAMED 28MM BIOCERAM-Z TOTAL HIP FEMORAL BALL | LZO | 1992-02-19 | View |
No matching devices.
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