Cleared Traditional

K990095 - STRAIGHT-IN-ORTHOPEDIC BONE SCREW FIXATION SYSTEM

K990095 is an FDA 510(k) clearance for STRAIGHT-IN-ORTHOPEDIC BONE SCREW FIXAT..., manufactured by Influence, Inc.. The device is a Class 2 Orthopedic device with product code MBI cleared through the Traditional 510(k) pathway after a 20-day FDA review.

K990095 · Influence, Inc. · Orthopedic device
Download Printable Device Report (PDF)
Optimized for regulatory review, auditing and printing
Feb 1999
Decision
20d
Days
Class 2
Risk

K990095 is an FDA 510(k) clearance for the STRAIGHT-IN-ORTHOPEDIC BONE SCREW FIXATION SYSTEM. Classified as Fastener, Fixation, Nondegradable, Soft Tissue within the MBI classification (a category for soft tissue fixation fasteners and anchoring systems), Class II - Special Controls.

Submitted by Influence, Inc. (Washington, US). The FDA issued a Cleared decision on February 1, 1999 after a review of 20 days - a notably fast clearance cycle.

This device falls under the Orthopedic FDA review panel, regulated under 21 CFR 888.3040 - 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 Influence, Inc. devices

FDA 510(k) Submission Details - K990095

510(k) Number K990095 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received January 12, 1999
Decision Date February 01, 1999
Days to Decision 20 days
Submission Type Traditional
Review Panel Orthopedic (OR)
Summary Summary PDF
Third-party Review No - reviewed directly by FDA
Combination Product No
PCCP Authorized No
Regulatory Context
Review time vs. panel average
102d faster than avg
Panel avg: 122d · This submission: 20d
Pathway characteristics
Predicate-based equivalence. No clinical trials required.

MBI Device Classification - Class 2, Special Controls

Product Code MBI Fastener, Fixation, Nondegradable, Soft Tissue
Device Class Class 2 - Special Controls
CFR Regulation 21 CFR 888.3040
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 - MBI Fastener, Fixation, Nondegradable, Soft Tissue

All 564
Devices cleared under the same product code (MBI) and FDA review panel - the closest regulatory comparables to K990095.
BONE ANCHOR SYSTEM III (BAS III)
K990295 · Boston Scientific Corp · Mar 1999
MICROTAC-BONE ANCHOR SYSTEM
K990160 · Influence, Inc. · Feb 1999
IMPLEX SCREW AND WASHER SYSTEM
K982751 · Implex Corp. · Feb 1999
INNOVASIVE DEVICES INTRATUNNEL TIBIAL FIXATION FASTENER
K983560 · Innovasive Devices, Inc. · Jan 1999
STABILIZER SOFT TISSUE ANCHOR, 5 AND 8MM
K984200 · R. Thomas Grotz, M.D., Inc. · Jan 1999
STRYKER WEDGE SUTURE ANCHOR
K983557 · Stryker Endoscopy · Dec 1998