Cleared Traditional

PRE-ROLLED TUBULAR STOCKINETTE (K831936) - FDA 510(k) Clearance

K831936 · Ormed Mfg., Inc. · General & Plastic Surgery device
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Dec 1983
Decision
198d
Days
-
Risk

K831936 is an FDA 510(k) clearance for the PRE-ROLLED TUBULAR STOCKINETTE.

Submitted by Ormed Mfg., Inc. (Mchenry, US). The FDA issued a Cleared decision on December 30, 1983 after a review of 198 days - an extended review cycle.

This device falls under the General & Plastic Surgery 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: Standard predicate-based submission. Standard predicate reliance. This clearance follows a standard predicate-based equivalence path within the General & Plastic Surgery review framework, consistent with the majority of Class II 510(k) submissions.

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Submission Details

510(k) Number K831936 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received June 15, 1983
Decision Date December 30, 1983
Days to Decision 198 days
Submission Type Traditional
Review Panel General & Plastic Surgery (SU)
Summary -
Third-party Review No - reviewed directly by FDA
Regulatory Context
Review time vs. panel average
83d slower than avg
Panel avg: 115d · This submission: 198d
Pathway characteristics
Predicate-based equivalence.

Device Classification

Product Code -
Device Class -