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
K842518Substantially Equivalent

Uniloc-Cementless & Self Tap Acetabular

American Ortomed Corp., Poughkeepsie NY / Traditional, Substantially Equivalent
FDA source (opens on fda.gov)

K842518 is the FDA 510(k) clearance record for UNILOC-CEMENTLESS & SELF TAP ACETABULAR, a class III device, cleared for American Ortomed Corp. on under FDA product code KWA (Prosthesis, Hip, Semi-Constrained (Metal Uncemented Acetabular Component)). FDA records list 6 510(k) clearances for American Ortomed Corp., from to . As of , FDA records show no recalls naming K842518.

Clearance record

Decision date
Received
(204 days to decision)
Product code
KWA Prosthesis, Hip, Semi-Constrained (Metal Uncemented Acetabular Component)
Regulation
21 CFR 888.3330
Device class
Class III
Review panel
Orthopedic
Applicant
American Ortomed Corp. P.O. Box 3184, Poughkeepsie NY
Third party review
No

Clearances, product code KWA

Trailing 12 months

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

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