510(K) CLEARANCES 84 ▲14RECALLS POSTED 39 ▲27CLASS I 6 ▲2PMA DECISIONS 47 ▲11WEEK ENDING / FDA DATA AS OF
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K912931Substantially Equivalent

Itm Sonic Surgery System

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

K912931 is the FDA 510(k) clearance record for ITM SONIC SURGERY SYSTEM, a class II device, cleared for Buckman Co., Inc. on under FDA product code JDX (Instrument, Surgical, Sonic And Accessory/Attachment). FDA records list 111 510(k) clearances for Buckman Co., Inc., from to . As of , FDA records show no recalls naming K912931.

Clearance record

Decision date
Received
(90 days to decision)
Product code
JDX Instrument, Surgical, Sonic And Accessory/Attachment
Regulation
21 CFR 888.4580
Device class
Class II
Review panel
Orthopedic
Applicant
Buckman Co., Inc. 1000 Burnett Ave., Suite 450, Concord CA
510(k) summary
Statement
Third party review
No

Clearances, product code JDX

Trailing 12 months

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

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