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

LEW MDI O-BALL COLLARED IMPLANT,

K Number: K121707 · Decision Sep 24, 2012
Classifications
1
FEI Numbers
324
Registration Numbers
324
Same Product Code
1545
Applicant Total
4
Review Days
105

Research this 510(k) in seconds

The Research Assistant summarizes clearance history, predicates and product-code trends — and cites every record.

Free to try · every answer cites its records

Basic Information

Device Name
LEW MDI O-BALL COLLARED IMPLANT,
K Number
K121707
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
872.3640
Medical Specialty
Dental
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Park Dental Research Corp.
Date Received
June 11, 2012
Decision Date
September 24, 2012
Product Code
DZE
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
DZE Implant, Endosseous, Root-Form

Similar 510(k) Clearances

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

View all

Other Clearances by Park Dental Research Corp.

K Number Device Name
K252976 Park Dental Nylon MAD
K082800 STAR/VENT INTERNAL HEX SCREW IMPLANT
K854749 STARTANIUS DENTAL IMPLANT SYSTEM