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FDA 510(k), K070598, MEMOMETAL INTRA-MEDULLARY BONE FASTENER, MODELS SMART TOE / X-FUSE
FDA 510(k), K070598, MEMOMETAL INTRA-MEDULLARY BONE FASTENER, MODELS SMART TOE / X-FUSE
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510(K) Number: K070598
Device Name: MEMOMETAL INTRA-MEDULLARY BONE FASTENER, MODELS SMART TOE / X-FUSE
Manufacturer: MEMOMETAL TECHNOLOGIES
Device Classification Name: pin, fixation, smooth
Regulation Number: 888.3040
Classification Product Code: HTY
Date Received: 03/02/2007
Decision Date: 07/26/2007
Regulation Medical Specialty: Orthopedic
Device Name: MEMOMETAL INTRA-MEDULLARY BONE FASTENER, MODELS SMART TOE / X-FUSE
Manufacturer: MEMOMETAL TECHNOLOGIES
Device Classification Name: pin, fixation, smooth
Regulation Number: 888.3040
Classification Product Code: HTY
Date Received: 03/02/2007
Decision Date: 07/26/2007
Regulation Medical Specialty: Orthopedic
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- Delivery: Approximately 1 to 2 weeks when the FOIA office is operating at regular capacity
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