510(K) CLEARANCES 84 ▲14RECALLS POSTED 39 ▲27CLASS I 6 ▲2PMA DECISIONS 47 ▲11WEEK ENDING / FDA DATA AS OF
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K093438Substantially Equivalent

Paradigm Interspinous Fusion Plate

Paradigm Spine GmbH, Washington DC / Traditional, Substantially Equivalent
FDA source (opens on fda.gov)510(k) summary (opens on fda.gov)

K093438 is the FDA 510(k) clearance record for PARADIGM INTERSPINOUS FUSION PLATE, a class II device, cleared for Paradigm Spine, LLC on under FDA product code KWP (Appliance, Fixation, Spinal Interlaminal). FDA records list 16 510(k) clearances for Paradigm Spine, LLC, from to . As of , FDA records show one recall naming K093438.

Clearance record

Decision date
Received
(336 days to decision)
Product code
KWP Appliance, Fixation, Spinal Interlaminal
Regulation
21 CFR 888.3050
Device class
Class II
Review panel
Orthopedic
Applicant
Paradigm Spine, LLC 1331 H St. NW, Washington DC
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