Cleared Traditional

K151347 - MIS Spine Frame Instrument Case

K151347 is an FDA 510(k) clearance for MIS Spine Frame Instrument Case, manufactured by Thompson Surgical Instruments. The device is a Class 2 General Hospital device with product code KCT cleared through the Traditional 510(k) pathway after a 149-day FDA review.

K151347 · Thompson Surgical Instruments · General Hospital
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Optimized for regulatory review, auditing and printing
Oct 2015
Decision
149d
Days
Class 2
Risk

K151347 is an FDA 510(k) clearance for the MIS Spine Frame Instrument Case. Classified as Sterilization Wrap Containers, Trays, Cassettes & Other Accessories (product code KCT), Class II - Special Controls.

Submitted by Thompson Surgical Instruments (Traverse City, US). The FDA issued a Cleared decision on October 16, 2015 after a review of 149 days - within the typical 510(k) review window.

This device falls under the General Hospital FDA review panel, regulated under 21 CFR 880.6850 - the FDA general hospital 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: Standard predicate-based submission. Standard predicate reliance. This clearance follows a standard predicate-based equivalence path within the General Hospital review framework, consistent with the majority of Class II 510(k) submissions.

View all Thompson Surgical Instruments devices

FDA 510(k) Submission Details - K151347

510(k) Number K151347 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received May 20, 2015
Decision Date October 16, 2015
Days to Decision 149 days
Submission Type Traditional
Review Panel General Hospital (HO)
Summary Summary PDF
Third-party Review No - reviewed directly by FDA
Regulatory Context
Review time vs. panel average
20d slower than avg
Panel avg: 129d · This submission: 149d
Pathway characteristics
Predicate-based equivalence. No clinical trials required.

KCT Device Classification - Class 2, Special Controls

Product Code KCT Sterilization Wrap Containers, Trays, Cassettes & Other Accessories
Device Class Class 2 - Special Controls
CFR Regulation 21 CFR 880.6850
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 Hospital devices follow this clearance model.

Regulatory Peers - KCT Sterilization Wrap Containers, Trays, Cassettes & Other Accessories

All 177
Devices cleared under the same product code (KCT) and FDA review panel - the closest regulatory comparables to K151347.
ENHANCE ALLOGRAFT WEDGE INSTRUMENT TRAY
K152969 · Conmed Corporation · Mar 2016
Medtronic Transportation/Sterilization Cassettes
K152241 · Medtronic Sofamor Danek USA, Inc. · Jan 2016
Endoscope Sterilization Tray
K151450 · Intuitive Surgical, Inc. · Jan 2016
SterilContainer S
K151242 · Aesculap, Inc. · Oct 2015
NuVasive Sterilization Trays
K143579 · Nu Vasive, Incorporated · Aug 2015
SterilContainer S
K143729 · Aesculap, Inc. · Aug 2015