Cleared Traditional

PROSTHESIS, TRAPEZIUM & TRAPEZIUM TRIAL (K770856) - FDA 510(k) Clearance

K770856 · Depuy, Inc. · Orthopedic device
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May 1977
Decision
14d
Days
-
Risk

K770856 is an FDA 510(k) clearance for the PROSTHESIS, TRAPEZIUM & TRAPEZIUM TRIAL.

Submitted by Depuy, Inc. (Mchenry, US). The FDA issued a Cleared decision on May 23, 1977 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 Depuy, Inc. devices

Submission Details

510(k) Number K770856 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received May 09, 1977
Decision Date May 23, 1977
Days to Decision 14 days
Submission Type Traditional
Review Panel Orthopedic (OR)
Summary -
Third-party Review No - reviewed directly by FDA
Combination Product No
PCCP Authorized No
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 -