Cleared Traditional

K101886 - DSC/ALF SPINAL SYSTEM

K101886 is an FDA 510(k) clearance for DSC/ALF SPINAL SYSTEM, manufactured by Sintea Plastek, LLC. The device is a Class 2 Orthopedic device with product code MQP cleared through the Traditional 510(k) pathway after a 380-day FDA review.

K101886 · Sintea Plastek, LLC · Orthopedic device
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Jul 2011
Decision
380d
Days
Class 2
Risk

K101886 is an FDA 510(k) clearance for the DSC/ALF SPINAL SYSTEM. Classified as Spinal Vertebral Body Replacement Device (product code MQP), Class II - Special Controls.

Submitted by Sintea Plastek, LLC (Miami Beach, US). The FDA issued a Cleared decision on July 21, 2011 after a review of 380 days - an unusually long review period, suggesting complex equivalence evaluation.

This device falls under the Orthopedic FDA review panel, regulated under 21 CFR 888.3060 - the FDA orthopedic device regulatory 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. Elevated predicate reliance profile. This clearance follows a standard predicate-based equivalence path within the Orthopedic review framework, consistent with the majority of Class II 510(k) submissions.

View all Sintea Plastek, LLC devices

FDA 510(k) Submission Details - K101886

510(k) Number K101886 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received July 06, 2010
Decision Date July 21, 2011
Days to Decision 380 days
Submission Type Traditional
Review Panel Orthopedic (OR)
Summary Summary PDF
Third-party Review No - reviewed directly by FDA
Regulatory Context
Review time vs. panel average
258d slower than avg
Panel avg: 122d · This submission: 380d
Pathway characteristics
Predicate-based equivalence. No clinical trials required.

MQP Device Classification - Class 2, Special Controls

Product Code MQP Spinal Vertebral Body Replacement Device
Device Class Class 2 - Special Controls
CFR Regulation 21 CFR 888.3060
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 Orthopedic devices follow this clearance model.

Regulatory Peers - MQP Spinal Vertebral Body Replacement Device

All 209
Devices cleared under the same product code (MQP) and FDA review panel - the closest regulatory comparables to K101886.
SYNTHES XRL
K103320 · Synthes Spine Co.Lp · Oct 2011
FORTIFY(TM) AND FORTIFY(TM)-R CORPECTOMY SPACERS
K112756 · Globus Medical, Inc. · Oct 2011
STAXX XDL SYSTEM
K102315 · Spine Wave, Inc. · Aug 2011
STAXXSD SYSTEM
K111469 · Spine Wave, Inc. · Jul 2011
BIOSPINE VBR SYSTEM
K110864 · Aesculap Implant Systems, LLC · Jun 2011
STAXX(R) XD SYSTEM
K102682 · Spine Wave, Inc. · Nov 2010