510(K) CLEARANCES 75 ▼9RECALLS POSTED 26 ▼13CLASS I 2 ▼4PMA DECISIONS 54 ▲7WEEK ENDING / FDA DATA AS OF
Medical Device
ManufacturingTHE TRADE PAPER OF THE FACTORY FLOOR
SUBSCRIBE / SIGN IN
K832899Substantially Equivalent

Zimmer Ossimeter

Zimmer GmbH, Mchenry IL / Traditional, Substantially Equivalent
FDA source (opens on fda.gov)

K832899 is the FDA 510(k) clearance record for ZIMMER OSSIMETER, a class I device, cleared for Zimmer, Inc. on under FDA product code FTY (Tape, Measuring, Rulers And Calipers). FDA records list 872 510(k) clearances for Zimmer, Inc., from to . As of , FDA records show no recalls naming K832899.

Clearance record

Decision date
Received
(46 days to decision)
Product code
FTY Tape, Measuring, Rulers And Calipers
Regulation
21 CFR 878.4800
Device class
Class I
Review panel
General, Plastic Surgery
Applicant
Zimmer, Inc. 803 N. Front St. Suite 3, Mchenry IL
Third party review
No

Clearances, product code FTY

Trailing 12 months

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

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