Cleared Traditional

K925776 - BRANEMARK SYSTEM INTERLOCKING ABUTMENT/...

K925776 is the FDA 510(k) clearance for BRANEMARK SYSTEM INTERLOCKING ABUTMENT/... by Nobelpharma USA, Inc.. It is a Class 2 Dental device (product code DZE) cleared through the Traditional 510(k) pathway after a 451-day FDA review.

K925776 · Nobelpharma USA, Inc. · Dental device
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Feb 1994
Decision
451d
Days
Class 2
Risk

K925776 is an FDA 510(k) clearance for the BRANEMARK SYSTEM INTERLOCKING ABUTMENT/GOLD CYLIND. Classified as Implant, Endosseous, Root-form (product code DZE), Class II - Special Controls.

Submitted by Nobelpharma USA, Inc. (Chicago, US). The FDA issued a Cleared decision on February 10, 1994 after a review of 451 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: High-complexity regulatory submission. Elevated predicate reliance profile. The extended review timeline suggests the FDA required additional documentation before confirming substantial equivalence - a pattern common in complex or first-of-kind Dental submissions.

View all Nobelpharma USA, Inc. devices

Submission Details

510(k) Number K925776 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received November 16, 1992
Decision Date February 10, 1994
Days to Decision 451 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
324d slower than avg
Panel avg: 127d · This submission: 451d
Pathway characteristics
Predicate-based equivalence. No clinical trials required.

Device Classification

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 674
Devices cleared under the same product code (DZE) and FDA review panel - the closest regulatory comparables to K925776.
STRYKER PRECISION DENTAL IMPLANT SYSTEM
K921805 · Stryker Instruments · Mar 1994
CONICAL ABUTMENT
K933462 · Implant Innovations, Inc. · Mar 1994
MINIBALL ABUTMENT
K930155 · Steri-Oss, Inc. · Feb 1994
HA-BIONTEGRATED DENTAL IMPLANT SYSTEMS
K914137 · Lifecore Biomedical, Inc. · Feb 1994
STERI-OSS TITANIUM SCREW SERIES IMPLANT
K923484 · Steri-Oss, Inc. · Dec 1993
STERI-OSS SCREW STYLE CP TITANIUM IMPLANT
K923695 · Steri-Oss, Inc. · Dec 1993