510(K) CLEARANCES 84 ▲14RECALLS POSTED 39 ▲27CLASS I 6 ▲2PMA DECISIONS 47 ▲11WEEK ENDING / FDA DATA AS OF
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K110039Substantially Equivalent

Biomet Sports Medicine Sternal Closure System

Biomet Sports Medicine, Warsaw IN / Traditional, Substantially Equivalent
FDA source (opens on fda.gov)510(k) summary (opens on fda.gov)

K110039 is the FDA 510(k) clearance record for BIOMET SPORTS MEDICINE STERNAL CLOSURE SYSTEM, a class II device, cleared for Biomet Sports Medicine on under FDA product code JDQ (Cerclage, Fixation). FDA records list 13 510(k) clearances for Biomet Sports Medicine, from to . As of , FDA records show no recalls naming K110039.

Clearance record

Decision date
Received
(117 days to decision)
Product code
JDQ Cerclage, Fixation
Regulation
21 CFR 888.3010
Device class
Class II
Review panel
Orthopedic
Applicant
Biomet Sports Medicine 56 E. Bell Dr.,, Warsaw IN
510(k) summary
Summary PDF
Third party review
No

Clearances, product code JDQ

Trailing 12 months
1 clearance under product code JDQ in the twelve months to October 2026, July 2026 the highest month at 1.
Show the numbers
Monthly 510(k) clearances under FDA product code JDQ, trailing twelve months
MonthClearances
November 20250
December 20250
January 20260
February 20260
March 20260
April 20260
May 20260
June 20260
July 20261
August 20260
September 20260
October 20260