INTERFERENCE SCREW

Screw, Fixation, Bone

CONCEPT, INC.

The following data is part of a premarket notification filed by Concept, Inc. with the FDA for Interference Screw.

Pre-market Notification Details

Device IDK874676
510k NumberK874676
Device Name:INTERFERENCE SCREW
ClassificationScrew, Fixation, Bone
Applicant CONCEPT, INC. 12707 U.S. 19 SOUTH Clearwater,  FL  33546
ContactLori Colvin
CorrespondentLori Colvin
CONCEPT, INC. 12707 U.S. 19 SOUTH Clearwater,  FL  33546
Product CodeHWC  
CFR Regulation Number888.3040 [🔎]
DecisionSubstantially Equivalent (SESE)
TypeTraditional
3rd Party ReviewedNo
Combination ProductNo
Date Received1987-11-13
Decision Date1988-03-07

NIH GUDID Devices

Device IdentifiersubmissionNumberSupplement
20845854015220 K874676 000
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20845854014094 K874676 000
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20845854013691 K874676 000
20845854013585 K874676 000
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20845854014155 K874676 000
20845854014216 K874676 000
20845854015213 K874676 000
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20845854014780 K874676 000
20845854014766 K874676 000
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20845854014483 K874676 000
20845854014384 K874676 000
20845854014278 K874676 000
20845854014261 K874676 000
10845854014837 K874676 000

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