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U.S. Department of Health and Human Services

Premarket Approval (PMA)
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Note: this medical device record is a supplement. The device description may have changed. Be sure to look at the original PMA to get an up-to-date view of this device.
 
Trade NameBAK INTERBODY FUSION SYSTEM
Classification Nameintervertebral fusion device with bone graft, lumbar
Generic Namelumbar interbody fusion instrumentation
Regulation Number888.3080
ApplicantSPINE-TECH, INC.
PMA NumberP950002
Supplement NumberS002
Date Received02/05/1997
Decision Date05/09/1997
Product Code
MAX[ Registered Establishments with MAX ]
Advisory Committee Orthopedic
Supplement Typereal-time process
Supplement Reason change design/components/specifications - other
Expedited Review Granted? No
Combination Product No
Approval Order Statement 
Approval of the addition of the following sizes to the bak product line: a) bak implants (minor diameter (mm) x length (mm)) 11x20, 11x24, 11x28, 11x32, 11x36; 13x24, 13x28, 13x32, 13x36, 13x40; 15x28, 15x32, 15x36, 15x40, 15x44; 17x20, 17x32, 17x36, 17x40, 17x44; 19x24, 19x28, 19x32, 19x36, 19x40, 19x44; 21x28, 21x32, 21x36, 21x40, 21x44; and (b) end caps (diameter (mm)) 11; 19; and 21.
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