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

LOCATOR IMPLANT ANCHOR ATTACHMENT SYSTEM

K Number: K083324 · Decision Feb 25, 2009
Classifications
1
FEI Numbers
382
Registration Numbers
382
Same Product Code
708
Applicant Total
14
Review Days
105

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Basic Information

Device Name
LOCATOR IMPLANT ANCHOR ATTACHMENT SYSTEM
K Number
K083324
Device Class
FDA class 2
Clearance Type
Special
Regulation Number
872.3630
Medical Specialty
Dental
Decision
Substantially Equivalent
Statement or Summary
Statement
Applicant
Zest Anchors, Inc.
Date Received
November 12, 2008
Decision Date
February 25, 2009
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 Zest Anchors, Inc.

K Number Device Name
K150295 LOCATOR RTx
K072878 MODIFICATION TO: LOCATOR IMPLANT ANCHOR
K042466 X-2 IMPLANT ABUTMENT; BAR MALE; DISTAL EXTENSION MALE
K033699 LOCATOR BAR FEMALE, LOCATOR LASER BAR FEMALE, LOCATOR BAR CAST-TO FEMALE, MODELS 08587, 08588, 08586
K994257 LOCATOR IMPLANT ANCHOR
K925849 ZEST IMPLANT ANCHOR
K934668 ZEST IMPLANT ANCHOR ADVANCED GENERATION (DENTAL)
K925700 ZEST ANCHOR ADVANCED GENERATION
K882063 MAGNE-DENT MAGNET/ZEST RETROFIT KEEPER
K861561 ZEST MARK II (STANDARD & MINI)
Search all 14 clearances from Zest Anchors, Inc. →