FDA 510(k) FDA class 2 Substantially Equivalent 🇺🇸 United States

QUICK TAP SELF DRILLING SCREW

K Number: K982927 · Decision Sep 8, 1998
Classifications
1
FEI Numbers
71
Registration Numbers
71
Same Product Code
79
Applicant Total
33
Review Days
19

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Basic Information

Device Name
QUICK TAP SELF DRILLING SCREW
K Number
K982927
Device Class
FDA class 2
Clearance Type
Special
Regulation Number
872.4880
Medical Specialty
Dental
Decision
Substantially Equivalent
Statement or Summary
Statement
Applicant
Kinamed, Inc.
Date Received
August 20, 1998
Decision Date
September 8, 1998
Product Code
DZL
Advisory Committee
Dental
Review Advisory Committee
DE
Third Party
N

Classifications

This FDA 510(k) entry is associated with 1 FDA classification via its product code.

Product Code Device Name
DZL Screw, Fixation, Intraosseous

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K032950 GEM INSET PATELLAR COMPONENT
K030256 ISO-ELASTIC CERCLAGE SYSTEM
K020764 NAVIPRO
K013982 KINEMATCH PATELLO-FEMORAL RESURFACING IMPALANT
K010101 GEM POSTERIOR STABILIZED TOTAL KNEE SYSTEM
K003347 ORTHOPILOT
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