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

PRIMACONNEX CAD/CAM ABUTMENT SYSTEM

K Number: K072241 · Decision Nov 9, 2007
Classifications
1
FEI Numbers
382
Registration Numbers
382
Same Product Code
708
Applicant Total
34
Review Days
88

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Basic Information

Device Name
PRIMACONNEX CAD/CAM ABUTMENT SYSTEM
K Number
K072241
Device Class
FDA class 2
Clearance Type
Abbreviated
Regulation Number
872.3630
Medical Specialty
Dental
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Lifecore Biomedical, Inc.
Date Received
August 13, 2007
Decision Date
November 9, 2007
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 Lifecore Biomedical, Inc.

K Number Device Name
K073032 PRIMACONNEX SD ESTHETIC CONTOUR ZI ABUTMENTS
K072768 RESTORE, STAGE-1, RENOVA PRIMASOLO AND PRIMACONNEX DENTAL IMPLANTS
K072572 PRIMACONNEX RD AND WD ESTHETIC CONTOUR ZI ABUTMENTS
K062876 PRIMACONNEX CERAMIC ABUTMENTS
K060530 SD CERAMIC COPING FOR QUICK ABUTMENT, LOCKING. MODEL 45301. RD CERAMIC COPING FOR QUICK ABUTMENT, LOCKING, MODEL 45302.
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. →