510(K) CLEARANCES 84 ▲14RECALLS POSTED 39 ▲27CLASS I 6 ▲2PMA DECISIONS 47 ▲11WEEK ENDING / FDA DATA AS OF
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K924940Substantially Equivalent for Some Indications

Femoral & Tibial Augment Block

Joint Medical Products Corp., Stamford CT / Traditional, Substantially Equivalent for Some Indications
FDA source (opens on fda.gov)

K924940 is the FDA 510(k) clearance record for FEMORAL & TIBIAL AUGMENT BLOCK, a class II device, cleared for Joint Medical Products Corp. on under FDA product code JWH (Prosthesis, Knee, Patellofemorotibial, Semi-Constrained, Cemented, Polymer/Metal/Polymer). FDA records list 33 510(k) clearances for Joint Medical Products Corp., from to . As of , FDA records show no recalls naming K924940.

Clearance record

Decision date
Received
(160 days to decision)
Product code
JWH Prosthesis, Knee, Patellofemorotibial, Semi-Constrained, Cemented, Polymer/Metal/Polymer
Regulation
21 CFR 888.3560
Device class
Class II
Review panel
Orthopedic
Applicant
Joint Medical Products Corp. 860 Canal St., Stamford CT
Third party review
No

Clearances, product code JWH

Trailing 12 months
14 clearances under product code JWH in the twelve months to October 2026, September 2026 the highest month at 6.
Show the numbers
Monthly 510(k) clearances under FDA product code JWH, trailing twelve months
MonthClearances
November 20251
December 20251
January 20261
February 20260
March 20260
April 20261
May 20260
June 20261
July 20262
August 20261
September 20266
October 20260