510(K) CLEARANCES 49 ▼18RECALLS POSTED 23 ▼3CLASS I 1 ▼1PMA DECISIONS 37 ▼3WEEK ENDING / FDA DATA AS OF
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K871250Substantially Equivalent

Intra-Articulated Arthro Power System

Richard Wolf Medical Instruments Corp., Rosemont IL / Traditional, Substantially Equivalent
FDA source (opens on fda.gov)

K871250 is the FDA 510(k) clearance record for INTRA-ARTICULATED ARTHRO POWER SYSTEM, a class I device, cleared for Richard Wolf Medical Instruments Corp. on under FDA product code KIT (Media And Components, Synthetic Cell And Tissue Culture). FDA records list 153 510(k) clearances for Richard Wolf Medical Instruments Corp., from to . As of , FDA records show no recalls naming K871250.

Clearance record

Decision date
Received
(28 days to decision)
Product code
KIT Media And Components, Synthetic Cell And Tissue Culture
Regulation
21 CFR 864.2220
Device class
Class I
Review panel
Hematology
Applicant
Richard Wolf Medical Instruments Corp. 7046 Lyndon Ave., Rosemont IL
Third party review
No

Clearances, product code KIT

Trailing 12 months

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

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