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

SD CERAMIC COPING FOR QUICK ABUTMENT, LOCKING. MODEL 45301. RD CERAMIC COPING FOR QUICK ABUTMENT, LOCKING, MODEL 45302.

K Number: K060530 · Decision May 22, 2006
Classifications
1
FEI Numbers
27
Registration Numbers
27
Same Product Code
38
Applicant Total
34
Review Days
83

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Basic Information

Device Name
SD CERAMIC COPING FOR QUICK ABUTMENT, LOCKING. MODEL 45301. RD CERAMIC COPING FOR QUICK ABUTMENT, LOCKING, MODEL 45302.
K Number
K060530
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
872.3920
Medical Specialty
Dental
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Lifecore Biomedical, Inc.
Date Received
February 28, 2006
Decision Date
May 22, 2006
Product Code
ELL
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
ELL Teeth, Porcelain

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Other Clearances by Lifecore Biomedical, Inc.

K Number Device Name
K073032 PRIMACONNEX SD ESTHETIC CONTOUR ZI ABUTMENTS
K072241 PRIMACONNEX CAD/CAM ABUTMENT SYSTEM
K072768 RESTORE, STAGE-1, RENOVA PRIMASOLO AND PRIMACONNEX DENTAL IMPLANTS
K072572 PRIMACONNEX RD AND WD ESTHETIC CONTOUR ZI ABUTMENTS
K062876 PRIMACONNEX CERAMIC ABUTMENTS
K053643 STAGE- 1 TEMPORARY/HEALING CAP, MODEL 42021-42026
K051614 PRIMACONNEX INTERNAL CONNECTION IMPLANT SYSTEM, PRIMACONNEX INTERNAL CONNECTION PROSTHETICS
K050506 PRIMASOLO ONE-PIECE IMPLANTS & HEALING CAPS
K041324 CALMATRIX CALCIUM SULFATE BONE GRAFT BINDER
K032774 RENOVA INTERNAL HEX IMPLANT SYSTEM
Search all 34 clearances from Lifecore Biomedical, Inc. →