510(K) CLEARANCES 84 ▲14RECALLS POSTED 39 ▲27CLASS I 6 ▲2PMA DECISIONS 47 ▲11WEEK ENDING / FDA DATA AS OF
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K013063Substantially Equivalent

Grip Lock Anchor, Model 411374

Medtronic Neuromodulation, Minneapolis MN / Traditional, Substantially Equivalent
FDA source (opens on fda.gov)

K013063 is the FDA 510(k) clearance record for GRIP LOCK ANCHOR, MODEL 411374, a class II device, cleared for Medtronic Neurological on under FDA product code GZB (Stimulator, Spinal-Cord, Implanted (Pain Relief)). FDA records list 3 510(k) clearances for MEDTRONIC NEUROMODULATION, from to . As of , FDA records show no recalls naming K013063.

Clearance record

Decision date
Received
(90 days to decision)
Product code
GZB Stimulator, Spinal-Cord, Implanted (Pain Relief)
Regulation
21 CFR 882.5880
Device class
Class II
Review panel
Neurology
Applicant
Medtronic Neurological 800 53rd Ave., NE, Minneapolis MN
510(k) summary
Summary
Third party review
No

Clearances, product code GZB

Trailing 12 months

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

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