510(K) CLEARANCES 84 ▲14RECALLS POSTED 39 ▲27CLASS I 6 ▲2PMA DECISIONS 47 ▲11WEEK ENDING / FDA DATA AS OF
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K872949Substantially Equivalent

Acromed Bone Plate Bender

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

K872949 is the FDA 510(k) clearance record for ACROMED BONE PLATE BENDER, a class I device, cleared for Buckman Co., Inc. on under FDA product code HXW (Bender). FDA records list 111 510(k) clearances for Buckman Co., Inc., from to . As of , FDA records show no recalls naming K872949.

Clearance record

Decision date
Received
(79 days to decision)
Product code
HXW Bender
Regulation
21 CFR 888.4540
Device class
Class I
Review panel
Orthopedic
Applicant
Buckman Co., Inc. 921 Calle Verde, Martinez CA
Third party review
No

Clearances, product code HXW

Trailing 12 months

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

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