510(K) CLEARANCES 84 ▲14RECALLS POSTED 39 ▲27CLASS I 6 ▲2PMA DECISIONS 47 ▲11WEEK ENDING / FDA DATA AS OF
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K873826Substantially Equivalent

Acromed/kaneda Anterior Spinal Instrumentation

Acromed Corp., Martinez CA / Traditional, Substantially Equivalent
FDA source (opens on fda.gov)

K873826 is the FDA 510(k) clearance record for ACROMED/KANEDA ANTERIOR SPINAL INSTRUMENTATION, a class II device, cleared for Acromed Corp. on under FDA product code KWQ (Appliance, Fixation, Spinal Intervertebral Body). FDA records list 41 510(k) clearances for Acromed Corp., from to . As of , FDA records show no recalls naming K873826.

Clearance record

Decision date
Received
(434 days to decision)
Product code
KWQ Appliance, Fixation, Spinal Intervertebral Body
Regulation
21 CFR 888.3060
Device class
Class II
Review panel
Orthopedic
Applicant
Acromed Corp. Buckman Company, Inc., Martinez CA
Third party review
No

Clearances, product code KWQ

Trailing 12 months
11 clearances under product code KWQ in the twelve months to October 2026, March 2026 the highest month at 3.
Show the numbers
Monthly 510(k) clearances under FDA product code KWQ, trailing twelve months
MonthClearances
November 20250
December 20251
January 20260
February 20262
March 20263
April 20261
May 20262
June 20260
July 20261
August 20260
September 20261
October 20260