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

SPI ONETIME DENTAL IMPLANT

K Number: K022038 · Decision Jul 15, 2002
Classifications
1
FEI Numbers
324
Registration Numbers
324
Same Product Code
1545
Applicant Total
4
Review Days
21

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Basic Information

Device Name
SPI ONETIME DENTAL IMPLANT
K Number
K022038
Device Class
FDA class 2
Clearance Type
Special
Regulation Number
872.3640
Medical Specialty
Dental
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Paxmed International
Date Received
June 24, 2002
Decision Date
July 15, 2002
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.

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Other Clearances by Paxmed International

K Number Device Name
K113568 MTA-FILLAPEX
K010467 UNIVERSAL DENTAL COPING (UDC)
K011223 QUANTUM VERSATILITY (QVS) DENTAL IMPLANT SYSTEM