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777
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616
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528
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522
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489
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485
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Intervertebral Fusion Device...
444
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438
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Search FDA 510(k) devices
510k Database
Manufacturers
CA
E.B.S., Inc.
Medical Device Manufacturer
·
CA , Canada
E.B.S., Inc. - FDA 510(k) Cleared Devices
3 submissions
·
3 cleared
·
Since 1987
3
Total
3
Cleared
0
Denied
FDA 510(k) Regulatory Record - E.B.S., Inc.
Cardiovascular
✕
3
devices
1-3 of 3
Filters
Cleared
Mar 07, 1988
BIOMA 5000
K880036
·
DRG
Cardiovascular
·
62d
Cleared
Dec 07, 1987
BIOMA 3500
K872370
·
KRC
Cardiovascular
·
171d
Cleared
Feb 19, 1987
BIOMA 2000
K862808
·
DXG
Cardiovascular
·
211d
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Cardiovascular
3