510(K) CLEARANCES 84 ▲14RECALLS POSTED 39 ▲27CLASS I 6 ▲2PMA DECISIONS 47 ▲11WEEK ENDING / FDA DATA AS OF
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K201314Substantially Equivalent

Restor3d Utility Wedge

restor3d, Inc., Durham NC / Traditional, Substantially Equivalent
FDA source (opens on fda.gov)510(k) summary (opens on fda.gov)

K201314 is the FDA 510(k) clearance record for Restor3d Utility Wedge, a class II device, cleared for Restor3D, 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 19 510(k) clearances for Restor3D, Inc., from to . As of , FDA records show no recalls naming K201314.

Clearance record

Decision date
Received
(395 days to decision)
Product code
PLF Bone Wedge
Regulation
21 CFR 888.3030
Device class
Class II
Review panel
Orthopedic
Applicant
Restor3D, Inc. 311 W. Corporation St., Durham NC
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