510(K) CLEARANCES 84 ▲14RECALLS POSTED 39 ▲27CLASS I 6 ▲2PMA DECISIONS 47 ▲11WEEK ENDING / FDA DATA AS OF
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K131810Substantially Equivalent

Osseus Black Diamond Pedicle Screw System

Osseus Fusion Systems LLC, Round Rock TX / Traditional, Substantially Equivalent
FDA source (opens on fda.gov)510(k) summary (opens on fda.gov)

K131810 is the FDA 510(k) clearance record for OSSEUS BLACK DIAMOND PEDICLE SCREW SYSTEM, a class II device, cleared for Osseus Fusion Systems, LLC on under FDA product code MNH (Orthosis, Spondylolisthesis Spinal Fixation). FDA records list 10 510(k) clearances for Osseus Fusion Systems, LLC, from to . As of , FDA records show no recalls naming K131810.

Clearance record

Decision date
Received
(50 days to decision)
Product code
MNH Orthosis, Spondylolisthesis Spinal Fixation
Regulation
21 CFR 888.3070
Device class
Class II
Review panel
Orthopedic
Applicant
Osseus Fusion Systems, LLC 1001 Oackwood Blvd., Round Rock TX
510(k) summary
Summary PDF
Third party review
No

Clearances, product code MNH

Trailing 12 months

FDA records hold no clearances under product code MNH in the trailing twelve months.

FDA records show no clearances under product code MNH in the twelve months to October 2026.
Show the numbers
Monthly 510(k) clearances under FDA product code MNH, trailing twelve months
MonthClearances
November 20250
December 20250
January 20260
February 20260
March 20260
April 20260
May 20260
June 20260
July 20260
August 20260
September 20260
October 20260