510(K) CLEARANCES 84 ▲14RECALLS POSTED 39 ▲27CLASS I 6 ▲2PMA DECISIONS 47 ▲11WEEK ENDING / FDA DATA AS OF
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K960473Substantially Equivalent

Aesculap Power System Handpiece

Aesculap Inc, South San Francisco CA / Traditional, Substantially Equivalent
FDA source (opens on fda.gov)

K960473 is the FDA 510(k) clearance record for AESCULAP POWER SYSTEM HANDPIECE, a class I device, cleared for Aesculap, Inc. on under FDA product code GET (Motor, Surgical Instrument, Pneumatic Powered). FDA records list 269 510(k) clearances for Aesculap, Inc., from to . As of , FDA records show no recalls naming K960473.

Clearance record

Decision date
Received
(35 days to decision)
Product code
GET Motor, Surgical Instrument, Pneumatic Powered
Regulation
21 CFR 878.4820
Device class
Class I
Review panel
General, Plastic Surgery
Applicant
Aesculap, Inc. 1000 Gateway Blvd., South San Francisco CA
510(k) summary
Summary
Third party review
No

Clearances, product code GET

Trailing 12 months

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

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