FDA 510(k) FDA class 2 Substantially Equivalent 🇿🇦 South Africa

Zaga Zygomatic System

K Number: K222497 · Decision Nov 9, 2022
Classifications
1
FEI Numbers
324
Registration Numbers
324
Same Product Code
1545
Applicant Total
19
Review Days
83

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Basic Information

Device Name
Zaga Zygomatic System
K Number
K222497
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
872.3640
Medical Specialty
Dental
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Southern Implants (Pty), Ltd.
Date Received
August 18, 2022
Decision Date
November 9, 2022
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

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Other Clearances by Southern Implants (Pty), Ltd.

K Number Device Name
K232726 External Hex Implant System
K232418 Single Platform SP1 Implant System
K230873 Angulated Screw Channel (ASC) Solution Abutments & SI-BASE Abutments
K222469 TIB Abutments
K222457 Provata Implant System
K210923 Southern Implants Instrument Trays
K193084 TIB Abutment System
K192651 ZAGA Zygomatic System
K191054 Southern Implants MAX Implant System
K191250 Southern Implants PEEK Abutments
Search all 19 clearances from Southern Implants (Pty), Ltd. →