Cleared Traditional

K961005 - SARGON IMMEDIATE LOAD IMPLANT

K961005 is an FDA 510(k) clearance for SARGON IMMEDIATE LOAD IMPLANT, manufactured by Graham & James. The device is a Class 2 Dental device with product code DZE cleared through the Traditional 510(k) pathway after a 55-day FDA review.

K961005 · Graham & James · Dental device
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May 1996
Decision
55d
Days
Class 2
Risk

K961005 is an FDA 510(k) clearance for the SARGON IMMEDIATE LOAD IMPLANT. Classified as Implant, Endosseous, Root-form (product code DZE), Class II - Special Controls.

Submitted by Graham & James (Washington, US). The FDA issued a Cleared decision on May 6, 1996 after a review of 55 days - a notably fast clearance cycle.

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: 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 Graham & James devices

FDA 510(k) Submission Details - K961005

510(k) Number K961005 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received March 12, 1996
Decision Date May 06, 1996
Days to Decision 55 days
Submission Type Traditional
Review Panel Dental (DE)
Summary Statement
Third-party Review No - reviewed directly by FDA
Combination Product No
PCCP Authorized No
Regulatory Context
Review time vs. panel average
72d faster than avg
Panel avg: 127d · This submission: 55d
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 1187
Devices cleared under the same product code (DZE) and FDA review panel - the closest regulatory comparables to K961005.
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