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1975
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1271
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1256
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1111
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1098
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1046
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981
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Screw, Fixation, Bone
970
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Search FDA 510(k) devices
510k Database
Manufacturers
DE
Solitec GmbH
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Medical Device Manufacturer
·
DE , Planegg
Solitec GmbH - FDA 510(k) Cleared Devices
3 submissions
·
3 cleared
·
Since 1983
3
Total
3
Cleared
0
Denied
FDA 510(k) Regulatory Record - Solitec GmbH
Physical Medicine
✕
1
devices
1-1 of 1
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Cleared
Jul 17, 1991
DERMALIGHT PSORACOMB
K903660
·
IOB
Physical Medicine
·
341d
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3
Radiology
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1