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

PrimeTaper EV Dental Implants Ø3.0, DS Implants abutments with EV connection (XS)

K Number: K220841 · Decision Nov 16, 2022
Classifications
1
FEI Numbers
324
Registration Numbers
324
Same Product Code
1545
Applicant Total
65
Review Days
238

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Basic Information

Device Name
PrimeTaper EV Dental Implants Ø3.0, DS Implants abutments with EV connection (XS)
K Number
K220841
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
872.3640
Medical Specialty
Dental
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Dentsply Sirona
Date Received
March 23, 2022
Decision Date
November 16, 2022
Product Code
DZE
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
DZE Implant, Endosseous, Root-Form

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