K924376 is an FDA 510(k) clearance for the ROOT CANAL POST. Classified as Pin, Retentive And Splinting, And Accessory Instruments (product code EBL), Class I - General Controls.
Submitted by The Thera Group (Westford, US). The FDA issued a Cleared decision on November 22, 1993 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 872.3740 - 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.
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