Cleared Traditional

K760953 - DEEP FREEZE SYSTEM (DFS-30)

K760953 is the FDA 510(k) clearance for DEEP FREEZE SYSTEM (DFS-30) by Spembly Medical , Ltd.. It is a Class 2 General & Plastic Surgery device (product code GEH) cleared through the Traditional 510(k) pathway after a 14-day FDA review.

K760953 · Spembly Medical , Ltd. · General & Plastic Surgery device
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Nov 1976
Decision
14d
Days
Class 2
Risk

K760953 is an FDA 510(k) clearance for the DEEP FREEZE SYSTEM (DFS-30). Classified as Unit, Cryosurgical, Accessories (product code GEH), Class II - Special Controls.

Submitted by Spembly Medical , Ltd. (Mchenry, US). The FDA issued a Cleared decision on November 16, 1976 after a review of 14 days - a notably fast clearance cycle.

This device falls under the General & Plastic Surgery FDA review panel, regulated under 21 CFR 878.4350 - the FDA general and plastic surgery device framework. 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 Spembly Medical , Ltd. devices

Submission Details

510(k) Number K760953 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received November 02, 1976
Decision Date November 16, 1976
Days to Decision 14 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
101d faster than avg
Panel avg: 115d · This submission: 14d
Pathway characteristics
Predicate-based equivalence. No clinical trials required.

Device Classification

Product Code GEH Unit, Cryosurgical, Accessories
Device Class Class 2 - Special Controls
CFR Regulation 21 CFR 878.4350
What this classification means

Class II devices require demonstration of substantial equivalence to a legally marketed predicate device. This pathway does not require clinical trials - it relies on engineering equivalence and performance data. Most General & Plastic Surgery devices follow this clearance model.