510(K) CLEARANCES 75 ▼9RECALLS POSTED 26 ▼13CLASS I 2 ▼4PMA DECISIONS 54 ▲7WEEK ENDING / FDA DATA AS OF
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K880402Substantially Equivalent

Codman Surgical Pattie

Cerenovus, Inc., Randolph MA / Traditional, Substantially Equivalent
FDA source (opens on fda.gov)

K880402 is the FDA 510(k) clearance record for CODMAN SURGICAL PATTIE, a class II device, cleared for Codman & Shurtleff, Inc. on under FDA product code HBA (Neurosurgical Paddie). FDA records list 163 510(k) clearances for Cerenovus, Inc., from to . As of , FDA records show 3 recalls naming K880402.

Clearance record

Decision date
Received
(33 days to decision)
Product code
HBA Neurosurgical Paddie
Regulation
21 CFR 882.4700
Device class
Class II
Review panel
Neurology
Applicant
Codman & Shurtleff, Inc. 41 Pacella Park Dr., Randolph MA
Third party review
No

Clearances, product code HBA

Trailing 12 months

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

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