510(K) CLEARANCES 84 ▲14RECALLS POSTED 39 ▲27CLASS I 6 ▲2PMA DECISIONS 47 ▲11WEEK ENDING / FDA DATA AS OF
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K012219Substantially Equivalent

Scalpfix Clip System

Aesculap Inc, Center Valley PA / Special, Substantially Equivalent
FDA source (opens on fda.gov)

K012219 is the FDA 510(k) clearance record for SCALPFIX CLIP SYSTEM, a class II device, cleared for Aesculap, Inc. on under FDA product code HBO (Clip, Scalp). FDA records list 269 510(k) clearances for Aesculap, Inc., from to . As of , FDA records show no recalls naming K012219.

Clearance record

Decision date
Received
(15 days to decision)
Product code
HBO Clip, Scalp
Regulation
21 CFR 882.4150
Device class
Class II
Review panel
Neurology
Applicant
Aesculap, Inc. 3773 Corporate Pkwy., Center Valley PA
510(k) summary
Summary
Third party review
No

Clearances, product code HBO

Trailing 12 months
1 clearance under product code HBO in the twelve months to October 2026, July 2026 the highest month at 1.
Show the numbers
Monthly 510(k) clearances under FDA product code HBO, trailing twelve months
MonthClearances
November 20250
December 20250
January 20260
February 20260
March 20260
April 20260
May 20260
June 20260
July 20261
August 20260
September 20260
October 20260