510(K) CLEARANCES 84 ▲14RECALLS POSTED 39 ▲27CLASS I 6 ▲2PMA DECISIONS 47 ▲11WEEK ENDING / FDA DATA AS OF
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K071633Substantially Equivalent

Lanx Deformity System

Lanx, LLC, Philadelphia PA / Special, Substantially Equivalent
FDA source (opens on fda.gov)510(k) summary (opens on fda.gov)

K071633 is the FDA 510(k) clearance record for LANX DEFORMITY SYSTEM, a class II device, cleared for Lanx, LLC on under FDA product code KWP (Appliance, Fixation, Spinal Interlaminal). FDA records list 4 510(k) clearances for Lanx, LLC, from to . As of , FDA records show no recalls naming K071633.

Clearance record

Decision date
Received
(62 days to decision)
Product code
KWP Appliance, Fixation, Spinal Interlaminal
Regulation
21 CFR 888.3050
Device class
Class II
Review panel
Orthopedic
Applicant
Lanx, LLC 1835 Market St., 28th Floor, Philadelphia PA
510(k) summary
Summary PDF
Third party review
No

Clearances, product code KWP

Trailing 12 months

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

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