510(K) CLEARANCES 84 ▲14RECALLS POSTED 39 ▲27CLASS I 6 ▲2PMA DECISIONS 47 ▲11WEEK ENDING / FDA DATA AS OF
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K811288Substantially Equivalent

Spetzler Lumbar-Peritoneal System

American Heyer Schulte, Mchenry IL / Traditional, Substantially Equivalent
FDA source (opens on fda.gov)

K811288 is the FDA 510(k) clearance record for SPETZLER LUMBAR-PERITONEAL SYSTEM, a class II device, cleared for American Heyer Schulte on under FDA product code JXG (Shunt, Central Nervous System And Components). FDA records list 13 510(k) clearances for American Heyer Schulte, from to . As of , FDA records show 5 recalls naming K811288.

Clearance record

Decision date
Received
(46 days to decision)
Product code
JXG Shunt, Central Nervous System And Components
Regulation
21 CFR 882.5550
Device class
Class II
Review panel
Neurology
Applicant
American Heyer Schulte 803 N. Front St. Suite 3, Mchenry IL
Third party review
No

Clearances, product code JXG

Trailing 12 months
4 clearances under product code JXG in the twelve months to October 2026, November 2025 the highest month at 2.
Show the numbers
Monthly 510(k) clearances under FDA product code JXG, trailing twelve months
MonthClearances
November 20252
December 20251
January 20260
February 20260
March 20260
April 20260
May 20260
June 20261
July 20260
August 20260
September 20260
October 20260