510(K) CLEARANCES 84 ▲14RECALLS POSTED 39 ▲27CLASS I 6 ▲2PMA DECISIONS 47 ▲11WEEK ENDING / FDA DATA AS OF
Medical Device
ManufacturingTHE TRADE PAPER OF THE FACTORY FLOOR
SUBSCRIBE / SIGN IN
K151256Substantially Equivalent

Arthrex BioSync® Bone Wedge

Arthex, Inc., Naples FL / Traditional, Substantially Equivalent
FDA source (opens on fda.gov)510(k) summary (opens on fda.gov)

K151256 is the FDA 510(k) clearance record for Arthrex BioSync® Bone Wedge, a class II device, cleared for Arthex, Inc. on under FDA product code PLF (Bone Wedge). FDA's definition for product code PLF reads: "Intended to be used with ancillary fixation for opening wedge osteotomies or fusion in the ankle, foot, proximal tibia". FDA records list 3 510(k) clearances for Arthex, Inc., from to . As of , FDA records show 6 recalls naming K151256.

Clearance record

Decision date
Received
(92 days to decision)
Product code
PLF Bone Wedge
Regulation
21 CFR 888.3030
Device class
Class II
Review panel
Orthopedic
Applicant
Arthex, Inc. 1370 Creekside Blvd., Naples FL
510(k) summary
Summary PDF
Third party review
No

Clearances, product code PLF

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