Cleared Traditional

K770501 - KNEE CUFF FOR EXPRESSING FLUID (FDA 510(k) Clearance)

K770501 · Robert R. Moore · Orthopedic device
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Apr 1977
Decision
21d
Days
-
Risk

K770501 is an FDA 510(k) clearance for the KNEE CUFF FOR EXPRESSING FLUID.

Submitted by Robert R. Moore (Walker, US). The FDA issued a Cleared decision on April 5, 1977 after a review of 21 days - a notably fast clearance cycle.

This device falls under the Orthopedic FDA review panel. 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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Submission Details

510(k) Number K770501 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received March 15, 1977
Decision Date April 05, 1977
Days to Decision 21 days
Submission Type Traditional
Review Panel Orthopedic (OR)
Summary -
Third-party Review No - reviewed directly by FDA
Regulatory Context
Review time vs. panel average
101d faster than avg
Panel avg: 122d · This submission: 21d
Pathway characteristics
Predicate-based equivalence.

Device Classification

Product Code -
Device Class -