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FDA 510(k), K051296, SIJF CANNULATED SCREW SYSTEM
FDA 510(k), K051296, SIJF CANNULATED SCREW SYSTEM
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510(K) Number: K051296
Device Name: SIJF CANNULATED SCREW SYSTEM
Manufacturer: DEPUY SPINE, INC.
Device Classification Name: sacroiliac joint fixation
Regulation Number: 888.3040
Classification Product Code: OUR
Date Received: 05/18/2005
Decision Date: 08/26/2005
Regulation Medical Specialty: Orthopedic
Device Name: SIJF CANNULATED SCREW SYSTEM
Manufacturer: DEPUY SPINE, INC.
Device Classification Name: sacroiliac joint fixation
Regulation Number: 888.3040
Classification Product Code: OUR
Date Received: 05/18/2005
Decision Date: 08/26/2005
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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