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
K062413Substantially Equivalent

Aesculap Pneumatic Kerrison

Aesculap Inc, Center Valley PA / Traditional, Substantially Equivalent
FDA source (opens on fda.gov)510(k) summary (opens on fda.gov)

K062413 is the FDA 510(k) clearance record for AESCULAP PNEUMATIC KERRISON, a class II device, cleared for Aesculap, Inc. on under FDA product code HAD (Rongeur, Powered). FDA records list 269 510(k) clearances for Aesculap, Inc., from to . As of , FDA records show no recalls naming K062413.

Clearance record

Decision date
Received
(96 days to decision)
Product code
HAD Rongeur, Powered
Regulation
21 CFR 882.4845
Device class
Class II
Review panel
Neurology
Applicant
Aesculap, Inc. 3773 Corporate Pkwy., Center Valley PA
510(k) summary
Summary PDF
Third party review
No

Clearances, product code HAD

Trailing 12 months

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

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