510(K) CLEARANCES 84 ▲14RECALLS POSTED 39 ▲27CLASS I 6 ▲2PMA DECISIONS 47 ▲11WEEK ENDING / FDA DATA AS OF
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K781443Substantially Equivalent

Harrington Spine Instrumentation

Orthopedic Equipment Co., Inc., Walker MI / Traditional, Substantially Equivalent
FDA source (opens on fda.gov)

K781443 is the FDA 510(k) clearance record for HARRINGTON SPINE INSTRUMENTATION, a class II device, cleared for Orthopedic Equipment Co., Inc. on under FDA product code KWP (Appliance, Fixation, Spinal Interlaminal). FDA records list 45 510(k) clearances for Orthopedic Equipment Co., Inc., from to . As of , FDA records show no recalls naming K781443.

Clearance record

Decision date
Received
(35 days to decision)
Product code
KWP Appliance, Fixation, Spinal Interlaminal
Regulation
21 CFR 888.3050
Device class
Class II
Review panel
Orthopedic
Applicant
Orthopedic Equipment Co., Inc. 4221 Richmond Rd., NW, Walker MI
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