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FDA 510(k) Applications for Medical Device Product Code "GEY"
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FDA 510(k) Number | Applicant | Device Name | Decision Date |
K020621 | ARTHROCARE CORP. | ARTHROCARE CONTROLLER; ARTHROCARE CABLE; FOOT CONTROL; POWER CORD; WANDS | 03/28/2002 |
K964073 | BIOMEDICAL ENT., INC. | BME BONE DRILL BITS | 11/14/1996 |
K961901 | BIOMEDICAL ENT., INC. | BONE & MARROW COLLECTION SYSTEM | 08/06/1996 |
K971782 | BIOMEDICAL ENT., INC. | BONE AND MARROW COLLECTION SYSTEM KIT | 07/29/1997 |
K971268 | BIOMEDICAL INTERNATIONAL CORP. | BONE & MARROW CLLECTION SYSTEM | 07/03/1997 |
K971941 | BOYD INDUSTRIES, INC. | AQUA SPRAY | 08/14/1997 |
K964252 | BUCKMAN CO., INC. | ORTHOCHUCK | 05/27/1997 |
K012738 | DEPUY ACROMED | SYMPHONY GRAFT DELIVERY SYSTEM (GDS) | 11/14/2001 |
K050519 | LINVATEC CORP. | ADVANCED TURBO DRIVE SYSTEM | 05/17/2005 |
K972308 | MEDNEXT, INC. | MEDNEXT 1000 DRILL | 08/20/1997 |
K962789 | SMITH & NEPHEW ENDOSCOPY, INC. | SURGICAL KIT-ACUFEX MOSAICPLASTY SYSTEM | 08/14/1996 |
K970530 | THE ANSPACH EFFORT, INC. | ANSPACH LUBRICATING SYSTEM II | 05/05/1997 |