K771418 is an FDA 510(k) clearance for the PIN RETRACTORS. Classified as Pin, Fixation, Smooth (product code HTY), Class II - Special Controls.
Submitted by Stryker Corp. (Mchenry, US). The FDA issued a Cleared decision on September 22, 1977 after a review of 52 days - a notably fast clearance cycle.
This device falls under the Orthopedic FDA review panel, regulated under 21 CFR 888.3040 - the FDA orthopedic 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.
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