FDA 510(k) Applications for Medical Device Product Code "GDY"
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FDA 510(k) Number | Applicant | Device Name | Decision Date |
K955599 | STRYKER CORP. | STRYKER FEMORAL CANAL SPONGE & ACETABULUM SPONGE | 02/22/1996 |
K972634 | ULTRACELL MEDICAL TECHNOLOGIES, INC. | ULTRACELL SUCTION SPONGE | 12/17/1997 |