510(K) CLEARANCES 84 ▲14RECALLS POSTED 39 ▲27CLASS I 6 ▲2PMA DECISIONS 47 ▲11WEEK ENDING / FDA DATA AS OF
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K112913Substantially Equivalent

Spotlight Access System

Johnson & Johnson, Raynham MA / Special, Substantially Equivalent
FDA source (opens on fda.gov)510(k) summary (opens on fda.gov)

K112913 is the FDA 510(k) clearance record for SPOTLIGHT ACCESS SYSTEM, a class II device, cleared for Johnson & Johnson on under FDA product code GZT (Retractor, Self-Retaining, For Neurosurgery). FDA records list 14 510(k) clearances for Johnson & Johnson, from to . As of , FDA records show no recalls naming K112913.

Clearance record

Decision date
Received
(74 days to decision)
Product code
GZT Retractor, Self-Retaining, For Neurosurgery
Regulation
21 CFR 882.4800
Device class
Class II
Review panel
Neurology
Applicant
Johnson & Johnson 325 Paramount Dr., Raynham MA
510(k) summary
Summary PDF
Third party review
No

Clearances, product code GZT

Trailing 12 months
1 clearance under product code GZT 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 GZT, 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