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

TruAbutment DS, TruBase S

K Number: K201197 · Decision Mar 26, 2021
Classifications
1
FEI Numbers
382
Registration Numbers
382
Same Product Code
708
Applicant Total
15
Review Days
326

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Basic Information

Device Name
TruAbutment DS, TruBase S
K Number
K201197
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
872.3630
Medical Specialty
Dental
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Truabutment, Inc.
Date Received
May 4, 2020
Decision Date
March 26, 2021
Product Code
NHA
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
NHA Abutment, Implant, Dental, Endosseous

Similar 510(k) Clearances

Other 510(k) clearances with the same product code (NHA), ordered by most recent decision date.

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Other Clearances by Truabutment, Inc.

K Number Device Name
K243255 URIS Long Implant & Abutments
K241485 TruAbutment DS; TruBase
K230438 URIS Smart Path Implant System & Prosthetic
K231874 AOT & T-L Abutment
K213961 TruAbutment DS, TruBase
K203649 TruAbutment DS, TruBase
K202579 TruAbutment DS, TruBase
K201842 TruBase S
K200817 URIS OMNI Narrow System & Prosthetic
K191913 TruAbutment DS
Search all 15 clearances from Truabutment, Inc. →