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

TSV BellaTek Encode Healing Abutments

K Number: K173374 · Decision Dec 13, 2017
Classifications
1
FEI Numbers
382
Registration Numbers
382
Same Product Code
708
Applicant Total
12
Review Days
47

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Basic Information

Device Name
TSV BellaTek Encode Healing Abutments
K Number
K173374
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
872.3630
Medical Specialty
Dental
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Biomet 3i
Date Received
October 27, 2017
Decision Date
December 13, 2017
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 Biomet 3i

K Number Device Name
K183138 Certain BellaTek Express and BellaTek Flex Abutments
K170013 Eztetic BellaTek Encode Healing Abutments
K150571 3i T3 Short Implants
K133049 3I T3(R) EXTERNAL HEX DENTAL IMPLANTS
K130949 CP4 OSSEOTITE CERTAIN DENTAL IMPLANTS
K130310 CERTAIN BELLATEK PROVISIONAL ABUTMENTS
K122300 T3 DENTAL IMPLANT
K120776 ABUTMENT FOR COMPETITIVE IMPLANT NOBEL ACTIVE CONNECTION
K112730 ABUTMENT FOR COMPETITIVE IMPLANT STRAUMANN BONE LEVEL CONNECTION
K110449 ENDOBON XENOGRAFT GRANULES
Search all 12 clearances from Biomet 3i →