510(K) CLEARANCES 75 ▼9RECALLS POSTED 26 ▼13CLASS I 2 ▼4PMA DECISIONS 54 ▲7WEEK ENDING / FDA DATA AS OF
Medical Device
ManufacturingTHE TRADE PAPER OF THE FACTORY FLOOR
SUBSCRIBE / SIGN IN
K063570Substantially Equivalent

Biomet Tibial Locking Nail System

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

K063570 is the FDA 510(k) clearance record for BIOMET TIBIAL LOCKING NAIL SYSTEM, a class II device, cleared for Biomet Manufacturing Corp on under FDA product code HSB (Rod, Fixation, Intramedullary And Accessories). FDA records list 128 510(k) clearances for Biomet Manufacturing Corp, from to . As of , FDA records show 3 recalls naming K063570.

Clearance record

Decision date
Received
(90 days to decision)
Product code
HSB Rod, Fixation, Intramedullary And Accessories
Regulation
21 CFR 888.3020
Device class
Class II
Review panel
Orthopedic
Applicant
Biomet Manufacturing Corp 56 E. Bell Dr.,, Warsaw IN
510(k) summary
Summary PDF
Third party review
No

Clearances, product code HSB

Trailing 12 months
19 clearances under product code HSB in the twelve months to October 2026, March 2026 the highest month at 7.
Show the numbers
Monthly 510(k) clearances under FDA product code HSB, trailing twelve months
MonthClearances
November 20250
December 20252
January 20260
February 20261
March 20267
April 20261
May 20262
June 20265
July 20260
August 20260
September 20261
October 20260