510(K) CLEARANCES 84 ▲14RECALLS POSTED 39 ▲27CLASS I 6 ▲2PMA DECISIONS 47 ▲11WEEK ENDING / FDA DATA AS OF
Medical Device
ManufacturingTHE TRADE PAPER OF THE FACTORY FLOOR
SUBSCRIBE / SIGN IN
K875054Substantially Equivalent

Acromed Ads Bone Nail Driver

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

K875054 is the FDA 510(k) clearance record for ACROMED ADS BONE NAIL DRIVER, a class I device, cleared for Buckman Co., Inc. on under FDA product code HWR (Driver, Prosthesis). FDA records list 111 510(k) clearances for Buckman Co., Inc., from to . As of , FDA records show no recalls naming K875054.

Clearance record

Decision date
Received
(50 days to decision)
Product code
HWR Driver, Prosthesis
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 HWR

Trailing 12 months

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

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