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

LOW PROFILE ABUTMENTS - INTERNAL AND EXTERNAL CONNECTION

K Number: K092341 · Decision Nov 30, 2009
Classifications
1
FEI Numbers
382
Registration Numbers
382
Same Product Code
708
Applicant Total
13
Review Days
118

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Basic Information

Device Name
LOW PROFILE ABUTMENTS - INTERNAL AND EXTERNAL CONNECTION
K Number
K092341
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, Inc.
Date Received
August 4, 2009
Decision Date
November 30, 2009
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

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Other Clearances by Biomet 3i, Inc.

K Number Device Name
K111216 OSSEOTITE 2 DENTAL IMPLANTS
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K100724 OSSEOTITE II MODEL XIFOSSXXX
K101607 BIOMET 3I PATIENT SPECIFIC DENTAL ABUTMENTS - ENCODE ABUTMENTS
K101608 BIOMET 3I PATIENT SPECIFIC DENTAL ABUTMENTS-ENCODE ABUTMENTS
K102209 ENCODE PATIENT SPECIFIC ABUTMENT
K101582 CAM STRUCTSURE BARS
K080864 CAM STRUCTSURE PRECISION MILLED BARS
K073345 CERTAIN CONTOURED MARGIN CERAMIC ABUTMENT
K072363 NANOTITE PREVAIL,CERTAIN,PARELLEL WALLED,TAPERED,EXTERNAL HEX
Search all 13 clearances from Biomet 3i, Inc. →