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477
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465
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433
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420
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389
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382
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Intervertebral Fusion Device...
355
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309
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302
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Manufacturers
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Pinook USA
Medical Device Manufacturer
·
US , San Diego , CA
Pinook USA - FDA 510(k) Cleared Devices
1 submissions
·
1 cleared
·
Since 2014
1
Total
1
Cleared
0
Denied
Pinook USA — FDA 510(k) Products and Clearance History
Neurology
✕
1
devices
1-1 of 1
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Cleared
Apr 24, 2014
PINOOK STIMULATOR
K132563
·
NUH
Neurology
·
252d
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Neurology
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