510(K) CLEARANCES 84 ▲14RECALLS POSTED 39 ▲27CLASS I 6 ▲2PMA DECISIONS 47 ▲11WEEK ENDING / FDA DATA AS OF
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K071931Substantially Equivalent

Codman Disposable Perforator, Model(s) 26-1222, 26-1223

Cerenovus, Inc., Raynham MA / Traditional, Substantially Equivalent
FDA source (opens on fda.gov)510(k) summary (opens on fda.gov)

K071931 is the FDA 510(k) clearance record for CODMAN DISPOSABLE PERFORATOR, MODEL(S) 26-1222, 26-1223, a class II device, cleared for Codman & Shurtleff, Inc. on under FDA product code HBF (Drills, Burrs, Trephines & Accessories (Compound, Powered)). FDA records list 163 510(k) clearances for Cerenovus, Inc., from to . As of , FDA records show no recalls naming K071931.

Clearance record

Decision date
Received
(101 days to decision)
Product code
HBF Drills, Burrs, Trephines & Accessories (Compound, Powered)
Regulation
21 CFR 882.4305
Device class
Class II
Review panel
Neurology
Applicant
Codman & Shurtleff, Inc. 325 Paramount Dr., Raynham MA
510(k) summary
Summary PDF
Third party review
No

Clearances, product code HBF

Trailing 12 months
1 clearance under product code HBF in the twelve months to October 2026, September 2026 the highest month at 1.
Show the numbers
Monthly 510(k) clearances under FDA product code HBF, 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 20261
October 20260