510(K) CLEARANCES 84 ▲14RECALLS POSTED 39 ▲27CLASS I 6 ▲2PMA DECISIONS 47 ▲11WEEK ENDING / FDA DATA AS OF
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K843950Substantially Equivalent

Link Cementless Screw-in Acetabular Cup

Waldemar Link GmbH & Co. KG, E. Hanover NJ / Traditional, Substantially Equivalent
FDA source (opens on fda.gov)

K843950 is the FDA 510(k) clearance record for LINK CEMENTLESS SCREW-IN ACETABULAR CUP, a class III device, cleared for Waldemar Link GmbH & Co. KG on under FDA product code KWA (Prosthesis, Hip, Semi-Constrained (Metal Uncemented Acetabular Component)). FDA records list 43 510(k) clearances for Waldemar Link GmbH & Co. KG, from to . As of , FDA records show no recalls naming K843950.

Clearance record

Decision date
Received
(237 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
Waldemar Link GmbH & Co. KG 10 Great Meadow Ln., E. Hanover NJ
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