Cleared Traditional

K770009 - BIOBOND C&B POST SOLDER

K770009 is an FDA 510(k) clearance for BIOBOND C&B POST SOLDER, manufactured by Dentsply Intl.. The device is a Class 2 Dental device with product code EJT cleared through the Traditional 510(k) pathway after a 11-day FDA review.

K770009 · Dentsply Intl. · Dental device
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Jan 1977
Decision
11d
Days
Class 2
Risk

K770009 is an FDA 510(k) clearance for the BIOBOND C&B POST SOLDER. Classified as Alloy, Gold-based Noble Metal (product code EJT), Class II - Special Controls.

Submitted by Dentsply Intl. (Mchenry, US). The FDA issued a Cleared decision on January 10, 1977 after a review of 11 days - a notably fast clearance cycle.

This device falls under the Dental FDA review panel, regulated under 21 CFR 872.3060 - 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 Dentsply Intl. devices

FDA 510(k) Submission Details - K770009

510(k) Number K770009 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received December 30, 1976
Decision Date January 10, 1977
Days to Decision 11 days
Submission Type Traditional
Review Panel Dental (DE)
Summary -
Third-party Review No - reviewed directly by FDA
Combination Product No
PCCP Authorized No
Regulatory Context
Review time vs. panel average
116d faster than avg
Panel avg: 127d · This submission: 11d
Pathway characteristics
Predicate-based equivalence. No clinical trials required.

EJT Device Classification - Class 2, Special Controls

Product Code EJT Alloy, Gold-based Noble Metal
Device Class Class 2 - Special Controls
CFR Regulation 21 CFR 872.3060
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 - EJT Alloy, Gold-based Noble Metal

All 551
Devices cleared under the same product code (EJT) and FDA review panel - the closest regulatory comparables to K770009.
A-33 DENTAL ALLOY
K781045 · Howmedica Corp. · Jul 1978
COLOR COTE
K771863 · Williams Gold Refining Co., Inc. · Oct 1977
HERITAGE SPECIAL ALLOY
K771110 · Howmedica Corp. · Jul 1977
SPIRAFLO DIALYZER, DISPOSABLE
K760797 · Bentley Laboratories, Inc. · Nov 1976
WILL-CERAM Y-2
K760122 · Williams Gold Refining Co., Inc. · Jul 1976