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

O-RING PROSTHETIC ATTACHMENT

K Number: K001638 · Decision Mar 4, 2002
Classifications
1
FEI Numbers
324
Registration Numbers
324
Same Product Code
1545
Applicant Total
2
Review Days
643

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Basic Information

Device Name
O-RING PROSTHETIC ATTACHMENT
K Number
K001638
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
872.3640
Medical Specialty
Dental
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Titan Implants
Date Received
May 30, 2000
Decision Date
March 4, 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

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Other Clearances by Titan Implants

K Number Device Name
K003818 TITANIUM ABUTMENT HEADS FOR IMZ IMPLANTS