510(K) CLEARANCES 84 ▲14RECALLS POSTED 39 ▲27CLASS I 6 ▲2PMA DECISIONS 47 ▲11WEEK ENDING / FDA DATA AS OF
Medical Device
ManufacturingTHE TRADE PAPER OF THE FACTORY FLOOR
SUBSCRIBE / SIGN IN
K811317Substantially Equivalent

Howmedica Femoral Pressuring Seal

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

K811317 is the FDA 510(k) clearance record for HOWMEDICA FEMORAL PRESSURING SEAL, a class I device, cleared for Howmedica Corp. on under FDA product code KIH (Dispenser, Cement). FDA records list 409 510(k) clearances for Howmedica Corp., from to . As of , FDA records show no recalls naming K811317.

Clearance record

Decision date
Received
(17 days to decision)
Product code
KIH Dispenser, Cement
Regulation
21 CFR 888.4200
Device class
Class I
Review panel
Orthopedic
Applicant
Howmedica Corp. 803 N. Front St. Suite 3, Mchenry IL
Third party review
No

Clearances, product code KIH

Trailing 12 months

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

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