Cleared Traditional

K133413 - IDSS SLC

K133413 is an FDA 510(k) clearance for IDSS SLC, manufactured by Black Diamond Video. The device is a Class 2 General & Plastic Surgery device with product code FTA cleared through the Traditional 510(k) pathway after a 61-day FDA review.

K133413 · Black Diamond Video · General & Plastic Surgery device
Download Printable Device Report (PDF)
Optimized for regulatory review, auditing and printing
Jan 2014
Decision
61d
Days
Class 2
Risk

K133413 is an FDA 510(k) clearance for the IDSS SLC. Classified as Light, Surgical, Accessories (product code FTA), Class II - Special Controls.

Submitted by Black Diamond Video (Richmond, US). The FDA issued a Cleared decision on January 7, 2014 after a review of 61 days - a notably fast clearance cycle.

This device falls under the General & Plastic Surgery FDA review panel, regulated under 21 CFR 878.4580 - 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 Black Diamond Video devices

FDA 510(k) Submission Details - K133413

510(k) Number K133413 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received November 07, 2013
Decision Date January 07, 2014
Days to Decision 61 days
Submission Type Traditional
Review Panel General & Plastic Surgery (SU)
Summary Summary PDF
Third-party Review No - reviewed directly by FDA
Regulatory Context
Review time vs. panel average
54d faster than avg
Panel avg: 115d · This submission: 61d
Pathway characteristics
Predicate-based equivalence. No clinical trials required.

FTA Device Classification - Class 2, Special Controls

Product Code FTA Light, Surgical, Accessories
Device Class Class 2 - Special Controls
CFR Regulation 21 CFR 878.4580
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.

Regulatory Peers - FTA Light, Surgical, Accessories

Devices cleared under the same product code (FTA) and FDA review panel - the closest regulatory comparables to K133413.
SCB/STERIS OR-LIGHT INTERFACE BOX
K051505 · KARL STORZ Endoscopy-America, Inc. · Aug 2005
KSEA SCB ACC CONTROL
K023704 · KARL STORZ Endoscopy-America, Inc. · Jan 2003
KSEA SCB MEDIA CONTROL
K020640 · KARL STORZ Endoscopy-America, Inc. · May 2002
CAM-WRAP
K810292 · Medline Industries, Inc. · Mar 1981
DIGAPHOT PHOTOTHERAPY METER MODEL PT 145
K780162 · Cavitron Corp. · Mar 1978