Cleared Traditional

K063734 - ATLANTIS ABUTMENT IN ZIRCONIA FOR 3I CE...

K063734 is an FDA 510(k) clearance for ATLANTIS ABUTMENT IN ZIRCONIA FOR 3I CE..., manufactured by Atlantis Components, Inc.. The device is a Class 2 Dental device with product code NHA cleared through the Traditional 510(k) pathway after a 74-day FDA review.

K063734 · Atlantis Components, Inc. · Dental device
Download Printable Device Report (PDF)
Optimized for regulatory review, auditing and printing
Mar 2007
Decision
74d
Days
Class 2
Risk

K063734 is an FDA 510(k) clearance for the ATLANTIS ABUTMENT IN ZIRCONIA FOR 3I CERTAIN INTERFACE. Classified as Abutment, Implant, Dental, Endosseous within the NHA classification (a category for dental implant abutments and prosthetic components), Class II - Special Controls.

Submitted by Atlantis Components, Inc. (Skokie, US). The FDA issued a Cleared decision on March 2, 2007 after a review of 74 days - a notably fast clearance cycle.

This device falls under the Dental FDA review panel, regulated under 21 CFR 872.3630 - the FDA dental device regulatory framework. The Traditional 510(k) pathway establishes clearance through substantial equivalence to a legally marketed predicate device, without requiring clinical trial data.

Device pattern: Fast-track predicate clearance. Standard predicate reliance. The short review cycle indicates strong predicate alignment - the FDA found sufficient equivalence without extended technical review.

View all Atlantis Components, Inc. devices

FDA 510(k) Submission Details - K063734

510(k) Number K063734 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received December 18, 2006
Decision Date March 02, 2007
Days to Decision 74 days
Submission Type Traditional
Review Panel Dental (DE)
Summary Summary PDF
Third-party Review No - reviewed directly by FDA
Combination Product No
PCCP Authorized No
Regulatory Context
Review time vs. panel average
53d faster than avg
Panel avg: 127d · This submission: 74d
Pathway characteristics
Predicate-based equivalence. No clinical trials required.

NHA Device Classification - Class 2, Special Controls

Product Code NHA Abutment, Implant, Dental, Endosseous
Device Class Class 2 - Special Controls
CFR Regulation 21 CFR 872.3630
Definition To Be Used In Conjunction With An Endosseous Dental Implant Fixture To Aid In Prosthetic Rehabilitation.
What this classification means

Class II devices require demonstration of substantial equivalence to a legally marketed predicate device. This pathway does not require clinical trials - it relies on engineering equivalence and performance data. Most Dental devices follow this clearance model.

Regulatory Peers - NHA Abutment, Implant, Dental, Endosseous

All 558
Devices cleared under the same product code (NHA) and FDA review panel - the closest regulatory comparables to K063734.
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K063592 · Nobel Biocare AB · Feb 2007
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K062069 · Atlantis Components, Inc. · Feb 2007