Cleared Traditional

COMPUTERIZED POSTURE PLATFORM (K771618) - FDA 510(k) Clearance

K771618 · Contraves Goerz Corp. · Ear, Nose, Throat device
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Sep 1977
Decision
19d
Days
-
Risk

K771618 is an FDA 510(k) clearance for the COMPUTERIZED POSTURE PLATFORM. Classified as Apparatus, Vestibular Analysis (product code LXV).

Submitted by Contraves Goerz Corp. (Mchenry, US). The FDA issued a Cleared decision on September 12, 1977 after a review of 19 days - a notably fast clearance cycle.

This device falls under the Ear, Nose, Throat 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 Contraves Goerz Corp. devices

Submission Details

510(k) Number K771618 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received August 24, 1977
Decision Date September 12, 1977
Days to Decision 19 days
Submission Type Traditional
Review Panel Ear, Nose, Throat (EN)
Summary -
Third-party Review No - reviewed directly by FDA
Regulatory Context
Review time vs. panel average
70d faster than avg
Panel avg: 89d · This submission: 19d
Pathway characteristics
Predicate-based equivalence.

Device Classification

Product Code LXV Apparatus, Vestibular Analysis
Device Class -