510(K) CLEARANCES 84 ▲14RECALLS POSTED 39 ▲27CLASS I 6 ▲2PMA DECISIONS 47 ▲11WEEK ENDING / FDA DATA AS OF
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K192945Substantially Equivalent

7D Surgical System Cranial Biopsy and Ventricular Catheter Placement Application

7D Surgical, Inc., Toronto, CA / Special, Substantially Equivalent
FDA source (opens on fda.gov)510(k) summary (opens on fda.gov)

K192945 is the FDA 510(k) clearance record for 7D Surgical System Cranial Biopsy and Ventricular Catheter Placement Application, a class II device, cleared for 7D Surgical, Inc. on under FDA product code HAW (Neurological Stereotaxic Instrument). FDA records list 10 510(k) clearances for 7D Surgical, Inc., from to . As of , FDA records show no recalls naming K192945.

Clearance record

Decision date
Received
(40 days to decision)
Product code
HAW Neurological Stereotaxic Instrument
Regulation
21 CFR 882.4560
Device class
Class II
Review panel
Neurology
Applicant
7D Surgical, Inc. 60 Scarsdale Rd., Unit 118, Toronto, CA
510(k) summary
Summary PDF
Third party review
No

Clearances, product code HAW

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