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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.
Classification Nameintervertebral fusion device with bone graft, lumbar
Generic Nameintervertebral cervical device
Regulation Number888.3080
PMA NumberP000028
Supplement NumberS001
Date Received07/09/2002
Decision Date08/13/2002
Product Code
MAX[ Registered Establishments with MAX ]
Advisory Committee Orthopedic
Supplement Typereal-time process
Supplement Reason labeling change - trade name
Expedited Review Granted? No
Combination Product No
Approval Order Statement 
Approval for the following changes to the device: 1) minor design changes to the cage, mainly consisting of minor changes to the threads; 2) provide the device sterile; and 3) change the device name to the affinity anterior cervical cage system. The device, as modified, will be marketed under the trade name affinity anterior cervical cage system and is indicated for anterior cervical interbody fusion procedures in skeletally mature patients with cervical disc disease at one level from the c2-c3 disc to the c7-t1 disc. Cervical disc disease is defined as intractable radiculopathy and/or myelopathy with herniated disc and/or osteophyte formation on posterior vertebral endplates producing symptomatic nerve root and/or spinal cord compression confirmed by radiographic studies. Affinity implants are to be used with autogenous bone graft and implanted via an open anterior approach.