510(K) CLEARANCES 84 ▲14RECALLS POSTED 39 ▲27CLASS I 6 ▲2PMA DECISIONS 47 ▲11WEEK ENDING / FDA DATA AS OF
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K801330Substantially Equivalent

Anspach Leg Support

The Anspach Effort, Inc., Mchenry IL / Traditional, Substantially Equivalent
FDA source (opens on fda.gov)

K801330 is the FDA 510(k) clearance record for ANSPACH LEG SUPPORT, a class I device, cleared for The Anspach Effort, Inc. on under FDA product code CCX (Support, Patient Position). FDA records list 60 510(k) clearances for The Anspach Effort, Inc., from to . As of , FDA records show no recalls naming K801330.

Clearance record

Decision date
Received
(23 days to decision)
Product code
CCX Support, Patient Position
Regulation
21 CFR 868.6820
Device class
Class I
Review panel
Anesthesiology
Applicant
The Anspach Effort, Inc. 803 N. Front St. Suite 3, Mchenry IL
Third party review
No

Clearances, product code CCX

Trailing 12 months

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

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