510(K) CLEARANCES 84 ▲14RECALLS POSTED 39 ▲27CLASS I 6 ▲2PMA DECISIONS 47 ▲11WEEK ENDING / FDA DATA AS OF
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K961732Substantially Equivalent

Kar

Landos, Inc., Potomac MD / Traditional, Substantially Equivalent
FDA source (opens on fda.gov)

K961732 is the FDA 510(k) clearance record for KAR, a class II device, cleared for Landos, Inc. on under FDA product code MEH (Prosthesis, Hip, Semi-Constrained, Uncemented, Metal / Polymer, Non-Porous, Calcium Phosphate). FDA records list 15 510(k) clearances for Landos, Inc., from to . As of , FDA records show no recalls naming K961732.

Clearance record

Decision date
Received
(431 days to decision)
Product code
MEH Prosthesis, Hip, Semi-Constrained, Uncemented, Metal / Polymer, Non-Porous, Calcium Phosphate
Regulation
21 CFR 888.3353
Device class
Class II
Review panel
Orthopedic
Applicant
Landos, Inc. 9109 Copenhaver Dr., Potomac MD
510(k) summary
Summary
Third party review
No

Clearances, product code MEH

Trailing 12 months
2 clearances under product code MEH in the twelve months to October 2026, November 2025 the highest month at 1.
Show the numbers
Monthly 510(k) clearances under FDA product code MEH, trailing twelve months
MonthClearances
November 20251
December 20250
January 20260
February 20260
March 20260
April 20260
May 20260
June 20260
July 20260
August 20261
September 20260
October 20260