510(K) CLEARANCES 84 ▲14RECALLS POSTED 39 ▲27CLASS I 6 ▲2PMA DECISIONS 47 ▲11WEEK ENDING / FDA DATA AS OF
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K926465Substantially Equivalent

Femoral Intramedullary Rods

Applied Osteo Systems, Inc., Walnut Creek CA / Traditional, Substantially Equivalent
FDA source (opens on fda.gov)

K926465 is the FDA 510(k) clearance record for FEMORAL INTRAMEDULLARY RODS, a class II device, cleared for Applied Osteo Systems, Inc. on under FDA product code JDS (Nail, Fixation, Bone). FDA records list 15 510(k) clearances for Applied Osteo Systems, Inc., from to . As of , FDA records show no recalls naming K926465.

Clearance record

Decision date
Received
(244 days to decision)
Product code
JDS Nail, Fixation, Bone
Regulation
21 CFR 888.3030
Device class
Class II
Review panel
Orthopedic
Applicant
Applied Osteo Systems, Inc. 1515 Oakland Blvd., Suite 110, Walnut Creek CA
510(k) summary
Summary
Third party review
No

Clearances, product code JDS

Trailing 12 months

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

FDA records show no clearances under product code JDS in the twelve months to October 2026.
Show the numbers
Monthly 510(k) clearances under FDA product code JDS, 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