Cleared Traditional

K130310 - CERTAIN BELLATEK PROVISIONAL ABUTMENTS

K130310 is an FDA 510(k) clearance for CERTAIN BELLATEK PROVISIONAL ABUTMENTS, manufactured by Biomet 3i. The device is a Class 2 Dental device with product code NHA cleared through the Traditional 510(k) pathway after a 134-day FDA review.

K130310 · Biomet 3i · Dental device
Download Printable Device Report (PDF)
Optimized for regulatory review, auditing and printing
Jun 2013
Decision
134d
Days
Class 2
Risk

K130310 is an FDA 510(k) clearance for the CERTAIN BELLATEK PROVISIONAL ABUTMENTS. 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 Biomet 3i (Palm Beach Gardens, US). The FDA issued a Cleared decision on June 21, 2013 after a review of 134 days - within the typical 510(k) review window.

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 Biomet 3i devices

FDA 510(k) Submission Details - K130310

510(k) Number K130310 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received February 07, 2013
Decision Date June 21, 2013
Days to Decision 134 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
7d slower than avg
Panel avg: 127d · This submission: 134d
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 651
Devices cleared under the same product code (NHA) and FDA review panel - the closest regulatory comparables to K130310.
ERA MICRO 23 FEMALE ABUTMENT, ERA MICRO 30 FEMALE ABUTMENT
K130408 · Sterngold Dental, LLC · Jul 2013
ET SMARTFIT ABUTMENT
K123627 · Hiossen, Inc. · Jun 2013
STRAUMANN HEALING ABUTMENTS, HEALING CAPS, CLOSURE SCREWS
K130808 · Straumann USA · Jun 2013
NOBELPROCERA PEEK ABUTMENTS
K120954 · Nobel Biocare AB · Jun 2013
BIODENTA DENTAL IMPLANT SYSTEM - MULTI-USE ABUTMENT
K123491 · Biodenta Swiss AG · May 2013
BIODENTA DENTAL IMPLANT SYSTEM - ABUTMENTS
K122559 · Biodenta Swiss AG · May 2013