Cleared Traditional

K934495 - BRANEMARK SYSTEM(R) UCLA-TYPE ABUTMENT COMPLETE

K934495 is an FDA 510(k) clearance for BRANEMARK SYSTEM UCLA-TYPE ABUTMENT COM..., manufactured by Nobelpharma AB. The device is a Class 2 Dental device with product code DZE cleared through the Traditional 510(k) pathway after a 328-day FDA review.

K934495 · Nobelpharma AB · Dental device
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Aug 1994
Decision
328d
Days
Class 2
Risk

K934495 is an FDA 510(k) clearance for the BRANEMARK SYSTEM(R) UCLA-TYPE ABUTMENT COMPLETE. Classified as Implant, Endosseous, Root-form (product code DZE), Class II - Special Controls.

Submitted by Nobelpharma AB (Chicago, US). The FDA issued a Cleared decision on August 8, 1994 after a review of 328 days - an unusually long review period, suggesting complex equivalence evaluation.

This device falls under the Dental FDA review panel, regulated under 21 CFR 872.3640 - 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. Elevated predicate reliance profile. 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 Nobelpharma AB devices

FDA 510(k) Submission Details - K934495

510(k) Number K934495 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received September 14, 1993
Decision Date August 08, 1994
Days to Decision 328 days
Submission Type Traditional
Review Panel Dental (DE)
Summary Summary PDF
Third-party Review No - reviewed directly by FDA
Regulatory Context
Review time vs. panel average
201d slower than avg
Panel avg: 127d · This submission: 328d
Pathway characteristics
Predicate-based equivalence. No clinical trials required.

DZE Device Classification - Class 2, Special Controls

Product Code DZE Implant, Endosseous, Root-form
Device Class Class 2 - Special Controls
CFR Regulation 21 CFR 872.3640
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 - DZE Implant, Endosseous, Root-form

All 1319
Devices cleared under the same product code (DZE) and FDA review panel - the closest regulatory comparables to K934495.
O BUTMENT ES IMPLANT
K923889 · "O" Co., Inc. · Aug 1994
HEXLOCK/HEXLOCK SCREW
K932168 · Imtec Corp. · Aug 1994
BRANEMARK SYSTEM DRILL CONTROLLER
K931785 · Nobelpharma USA, Inc. · Aug 1994
BRANEMARK SYSTEM
K934825 · Nobelpharma USA, Inc. · Aug 1994
BRANEMARK-HEALING CAPS, DCC045, DCC046, DCC104
K934826 · Nobelpharma USA, Inc. · Aug 1994
BRANEMARK SYSTEM ESTHETICONE NON-ROTATIONAL SYSTEM
K934827 · Nobelpharma USA, Inc. · Aug 1994