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FDA 510(k), K924724, KINETIK GREAT TOE SYSTEM
FDA 510(k), K924724, KINETIK GREAT TOE SYSTEM
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510(K) Number: K924724
Device Name: KINETIK GREAT TOE SYSTEM
Manufacturer: KINETIKOS MEDICAL, INC.
Device Classification Name: prosthesis, toe (metatarsophalangeal), joint, metal/polymer, semi-constrained
Regulation Number:
Classification Product Code: LZJ
Date Received: 09/21/1992
Decision Date: 01/05/1994
Regulation Medical Specialty:
Device Name: KINETIK GREAT TOE SYSTEM
Manufacturer: KINETIKOS MEDICAL, INC.
Device Classification Name: prosthesis, toe (metatarsophalangeal), joint, metal/polymer, semi-constrained
Regulation Number:
Classification Product Code: LZJ
Date Received: 09/21/1992
Decision Date: 01/05/1994
Regulation Medical Specialty:
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- Delivery: Approximately 1 to 2 weeks when the FOIA office is operating at regular capacity
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