Cleared Traditional

K160784 - CAM Titanium Blanks

K160784 is an FDA 510(k) clearance for CAM Titanium Blanks, manufactured by Altatec GmbH. The device is a Class 2 Dental device with product code NHA cleared through the Traditional 510(k) pathway after a 176-day FDA review.

K160784 · Altatec GmbH · Dental device
Download Printable Device Report (PDF)
Optimized for regulatory review, auditing and printing
Sep 2016
Decision
176d
Days
Class 2
Risk

K160784 is an FDA 510(k) clearance for the CAM Titanium Blanks. 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 Altatec GmbH (Wimsheim, DE). The FDA issued a Cleared decision on September 14, 2016 after a review of 176 days - an extended review 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: Standard predicate-based submission. Standard predicate reliance. This clearance follows a standard predicate-based equivalence path within the Dental review framework, consistent with the majority of Class II 510(k) submissions.

View all Altatec GmbH devices

FDA 510(k) Submission Details - K160784

510(k) Number K160784 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received March 22, 2016
Decision Date September 14, 2016
Days to Decision 176 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
49d slower than avg
Panel avg: 127d · This submission: 176d
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 Consultant

PaxMed International, LLC
LINDA K. SCHULZ

The regulatory consultant manages the 510(k) submission process on behalf of the applicant - coordinating technical documentation, predicate strategy and FDA communications. Identifying the consultant behind a submission is a key signal for competitive regulatory intelligence.

Regulatory Peers - NHA Abutment, Implant, Dental, Endosseous

All 653
Devices cleared under the same product code (NHA) and FDA review panel - the closest regulatory comparables to K160784.
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K160207 · Dentsply International, Inc. · Sep 2016
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K160964 · Jjgc Industria E Comercio DE Materiais Dentarios S.A. · Sep 2016
Dentium Implantium & SuperLine Prosthetics
K160828 · Dentium Co., Ltd. · Sep 2016
ATLANTIS Abutment for HIOSSEN ET implant
K160626 · Dentsply Sirona · Aug 2016
GPS Angled Abutment
K153509 · Implant Direct Sybron Manufacturing, LLC · Aug 2016
ATLANTIS Abutment for CONELOG implant
K161030 · Dentsply Sirona · Aug 2016