Cleared Traditional

K875290 - LUMBAR IMPACTION SET

K875290 is an FDA 510(k) clearance for LUMBAR IMPACTION SET, manufactured by T. Korossurgical Instruments Corp.. The device is a Class 2 Orthopedic device with product code KWP cleared through the Traditional 510(k) pathway after a 65-day FDA review.

K875290 · T. Korossurgical Instruments Corp. · Orthopedic device
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Mar 1988
Decision
65d
Days
Class 2
Risk

K875290 is an FDA 510(k) clearance for the LUMBAR IMPACTION SET. Classified as Appliance, Fixation, Spinal Interlaminal (product code KWP), Class II - Special Controls.

Submitted by T. Korossurgical Instruments Corp. (Moorepark, US). The FDA issued a Cleared decision on March 4, 1988 after a review of 65 days - a notably fast clearance cycle.

This device falls under the Orthopedic FDA review panel, regulated under 21 CFR 888.3050 - 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: 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 T. Korossurgical Instruments Corp. devices

FDA 510(k) Submission Details - K875290

510(k) Number K875290 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received December 30, 1987
Decision Date March 04, 1988
Days to Decision 65 days
Submission Type Traditional
Review Panel Orthopedic (OR)
Summary -
Third-party Review No - reviewed directly by FDA
Combination Product No
PCCP Authorized No
Regulatory Context
Review time vs. panel average
57d faster than avg
Panel avg: 122d · This submission: 65d
Pathway characteristics
Predicate-based equivalence. No clinical trials required.

KWP Device Classification - Class 2, Special Controls

Product Code KWP Appliance, Fixation, Spinal Interlaminal
Device Class Class 2 - Special Controls
CFR Regulation 21 CFR 888.3050
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 - KWP Appliance, Fixation, Spinal Interlaminal

All 282
Devices cleared under the same product code (KWP) and FDA review panel - the closest regulatory comparables to K875290.
MODULAR SPINAL FIXATION & LOCKING HOOK SPINAL ROD
K884688 · Synthes (Usa) · Feb 1989
LEA PLAZA SPINAL FRAME SYSTEM
K884585 · Orthomet, Inc. · Jan 1989
ROGOZINSKI SPINAL SYSTEM
K884263 · Richards Medical Co., Inc. · Dec 1988
ACROMED CROSS ROD CONNECTOR
K874882 · Acromed Corp. · Feb 1988
KIRSCHNER SPINAL PRODUCT SYSTEM
K854524 · Kirschner Medical Corp. · Dec 1985
EDWARDS SACRAL SCREW
K851935 · Zimmer, Inc. · Jun 1985