510(K) CLEARANCES 84 ▲14RECALLS POSTED 39 ▲27CLASS I 6 ▲2PMA DECISIONS 47 ▲11WEEK ENDING / FDA DATA AS OF
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K760002Substantially Equivalent

Knee Aid

Zimmer GmbH, 1831 Olive St. St. Louis MO / Traditional, Substantially Equivalent
FDA source (opens on fda.gov)

K760002 is the FDA 510(k) clearance record for KNEE AID, a class I device, cleared for Zimmer, Inc. on under FDA product code IQI (Orthosis, Limb Brace). FDA records list 872 510(k) clearances for Zimmer, Inc., from to . As of , FDA records show no recalls naming K760002.

Clearance record

Decision date
Received
(61 days to decision)
Product code
IQI Orthosis, Limb Brace
Regulation
21 CFR 890.3475
Device class
Class I
Review panel
Physical Medicine
Applicant
Zimmer, Inc.
Third party review
No

Clearances, product code IQI

Trailing 12 months

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

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