510(K) CLEARANCES 84 ▲14RECALLS POSTED 39 ▲27CLASS I 6 ▲2PMA DECISIONS 47 ▲11WEEK ENDING / FDA DATA AS OF
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K140908Substantially Equivalent

Juggerknot Mini Soft Anchor

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

K140908 is the FDA 510(k) clearance record for JUGGERKNOT MINI SOFT ANCHOR, a class II device, cleared for Biomet Sports Medicine on under FDA product code DZL (Screw, Fixation, Intraosseous). FDA records list 13 510(k) clearances for Biomet Sports Medicine, from to . As of , FDA records show no recalls naming K140908.

Clearance record

Decision date
Received
(176 days to decision)
Product code
DZL Screw, Fixation, Intraosseous
Regulation
21 CFR 872.4880
Device class
Class II
Review panel
Dental
Applicant
Biomet Sports Medicine 56 E. Bell Dr., Warsaw IN
510(k) summary
Summary PDF
Third party review
No

Clearances, product code DZL

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