510(K) CLEARANCES 84 ▲14RECALLS POSTED 39 ▲27CLASS I 6 ▲2PMA DECISIONS 47 ▲11WEEK ENDING / FDA DATA AS OF
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K935950Substantially Equivalent for Some Indications

Fx-Cablelok Cable/plate System

Buckman Co., Inc., Concord CA / Traditional, Substantially Equivalent for Some Indications
FDA source (opens on fda.gov)

K935950 is the FDA 510(k) clearance record for FX-CABLELOK CABLE/PLATE SYSTEM, a class II device, cleared for Buckman Co., Inc. on under FDA product code JDQ (Cerclage, Fixation). FDA records list 111 510(k) clearances for Buckman Co., Inc., from to . As of , FDA records show no recalls naming K935950.

Clearance record

Decision date
Received
(86 days to decision)
Product code
JDQ Cerclage, Fixation
Regulation
21 CFR 888.3010
Device class
Class II
Review panel
Orthopedic
Applicant
Buckman Co., Inc. 100 Burnett Ave., Concord CA
Third party review
No

Clearances, product code JDQ

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