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

OCO DENTAL IMPLANT

K Number: K021460 · Decision May 22, 2002
Classifications
1
FEI Numbers
382
Registration Numbers
382
Same Product Code
708
Applicant Total
17
Review Days
15

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Basic Information

Device Name
OCO DENTAL IMPLANT
K Number
K021460
Device Class
FDA class 2
Clearance Type
Special
Regulation Number
872.3630
Medical Specialty
Dental
Decision
Substantially Equivalent
Statement or Summary
Statement
Applicant
O Co., Inc.
Date Received
May 7, 2002
Decision Date
May 22, 2002
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 O Co., Inc.

K Number Device Name
K033392 IMMEDIATE STABILIZING IMPLANT (ISI)
K023336 OCO DENTAL IMPLANT (5.0MM DIAMETER)
K011524 IMMEDIATE STABILIZING DEVICE (ISD)
K010142 OCO DENTAL IMPLANT
K973926 O BUTMENT HS IMPLANT
K961665 O BUTMENT ET IMPLANT
K950066 DENTAL IMPLANT ENDOSSEOUS
K946113 IMPLANT BODY RETRIEVER/REMOVER
K946129 IMPLANT BODY DEPTH GAUGE/TRYIN
K945300 ACCESSORY ITEM TO ENDOSSEOUS DENTAL IMPLANT
Search all 17 clearances from O Co., Inc. →