Cleared Traditional

K961736 - 17 ANGULATED ABUTMENT

K961736 is the FDA 510(k) clearance for 17 ANGULATED ABUTMENT by Nobelpharma USA, Inc.. It is a Class 2 Dental device (product code NHA) cleared through the Traditional 510(k) pathway after a 76-day FDA review.

K961736 · Nobelpharma USA, Inc. · Dental device
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Optimized for regulatory review, auditing and printing
Jul 1996
Decision
76d
Days
Class 2
Risk

K961736 is an FDA 510(k) clearance for the 17 ANGULATED ABUTMENT. 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 Nobelpharma USA, Inc. (Westmont, US). The FDA issued a Cleared decision on July 18, 1996 after a review of 76 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 Nobelpharma USA, Inc. devices

Submission Details

510(k) Number K961736 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received May 03, 1996
Decision Date July 18, 1996
Days to Decision 76 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
51d faster than avg
Panel avg: 127d · This submission: 76d
Pathway characteristics
Predicate-based equivalence. No clinical trials required.

Device Classification

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 480
Devices cleared under the same product code (NHA) and FDA review panel - the closest regulatory comparables to K961736.
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K972475 · Nobel Biocare Uas, Inc. · Sep 1997
TIADAPT ABUTMENT SYSTEM
K971706 · Nobel Biocare Uas, Inc. · Jul 1997
BIO-ESTHETIC INDIRECT ABUTMENT
K970073 · Steri-Oss, Inc. · Jul 1997
MIRUSCONE ABUTMENT SYSTEM
K961728 · Nobelpharma USA, Inc. · Jul 1996
BRANEMARK SYSTEM TITANIUM HEALING ABUTMENTS
K925779 · Nobelpharma USA, Inc. · Apr 1993
BRANEMARK SYSTEM ABUTMENTS COMPLETE
K925769 · Nobelpharma USA, Inc. · Apr 1993