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535
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520
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493
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489
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431
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Intervertebral Fusion Device...
406
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400
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Manufacturers
US
Mecta Corp.
Medical Device Manufacturer
·
US , Portland , OR
Mecta Corp. - FDA 510(k) Cleared Devices
3 submissions
·
3 cleared
·
Since 1985
3
Total
3
Cleared
0
Denied
FDA 510(k) Regulatory Record - Mecta Corp.
Neurology
✕
3
devices
1-3 of 3
Filters
Cleared
Mar 06, 1997
SPECTRUM 5000 Q, 5000Q,M,4000 Q, 4000 M.
K965070
·
QGH
Neurology
·
85d
Cleared
Sep 18, 1996
SPECTRUM 5000 Q, 5000 M, 4000 Q, 4000 M
K960754
·
QGH
Neurology
·
208d
Cleared
Aug 09, 1985
MECTA ECT DEVICE MODELS SR & JR
K852069
·
QGH
Neurology
·
91d
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3
Neurology
3