Cleared Traditional

K810644 - HOFFMAN HOOP DEVICE (FDA 510(k) Clearance)

K810644 · Howmedica Corp. · Orthopedic device
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Mar 1981
Decision
14d
Days
-
Risk

K810644 is an FDA 510(k) clearance for the HOFFMAN HOOP DEVICE.

Submitted by Howmedica Corp. (Mchenry, US). The FDA issued a Cleared decision on March 24, 1981 after a review of 14 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.

View all Howmedica Corp. devices

Submission Details

510(k) Number K810644 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received March 10, 1981
Decision Date March 24, 1981
Days to Decision 14 days
Submission Type Traditional
Review Panel Orthopedic (OR)
Summary -
Third-party Review No - reviewed directly by FDA
Regulatory Context
Review time vs. panel average
108d faster than avg
Panel avg: 122d · This submission: 14d
Pathway characteristics
Predicate-based equivalence.

Device Classification

Product Code -
Device Class -