Cleared Traditional

K231236 - IBS-B MIS Beveled Screw System (FDA 510(k) Clearance)

Jul 2023
Decision
90d
Days
Class 2
Risk

K231236 is an FDA 510(k) clearance for the IBS-B MIS Beveled Screw System. This device is classified as a Screw, Fixation, Bone (Class II - Special Controls, product code HWC).

Submitted by In2bones USA, LLC (Memphis, US). The FDA issued a Cleared decision on July 27, 2023, 90 days after receiving the submission on April 28, 2023.

This device falls under the Orthopedic FDA review panel. Regulated under 21 CFR 888.3040.

Submission Details

510(k) Number K231236 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received April 28, 2023
Decision Date July 27, 2023
Days to Decision 90 days
Submission Type Traditional
Review Panel Orthopedic (OR)
Summary Summary PDF

Device Classification

Product Code HWC — Screw, Fixation, Bone
Device Class Class II - Special Controls
CFR Regulation 21 CFR 888.3040

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