Home › Device types › GYK
Instrument, Shunt System Implantation
FDA product code GYK · Class 1 · Neurology
61
Registered devices
15
Adverse events
1
Recalls
13
510(k) clearances
Devices with this code
CODMAN® — INTEGRA LIFESCIENCES PRODUCTION CORPORATIONPrecision Tunneler - Small — ARKIS BIOSCIENCES INC.CODMAN — Cerenovus, Inc.CODMAN® — INTEGRA LIFESCIENCES PRODUCTION CORPORATIONPhoenix Neuro — SOPHYSASubcutaneous Guidewire - Large — ARKIS BIOSCIENCES INC.Sophysa — SOPHYSANatus® — NATUS MEDICAL INCORPORATEDAESCULAP — Aesculap AGNatus® — NATUS MEDICAL INCORPORATEDSingle Pass Tunneling Guidewire - Medium — ARKIS BIOSCIENCES INC.CODMAN® — INTEGRA LIFESCIENCES PRODUCTION CORPORATIONIntegra® — INTEGRA NEUROSCIENCES IMPLANT (FRANCE)NA — MEDTRONIC PS MEDICAL, INC.N/A — MEDTRONIC PS MEDICAL, INC.CODMAN® — INTEGRA LIFESCIENCES PRODUCTION CORPORATIONPhoenix Neuro — SOPHYSAV. Mueller — CAREFUSION 2200, INCSophysa — SOPHYSACODMAN® — INTEGRA LIFESCIENCES PRODUCTION CORPORATIONNatus® — NATUS MEDICAL INCORPORATEDV. Mueller — CAREFUSION 2200, INCSophysa — SOPHYSAAESCULAP — Aesculap AG
Recent recalls
| Date | Firm | Reason |
|---|---|---|
| 2010-12-22 | Integra LifeSciences Corp. | Peritoneal Introducer Sheaths were incorrectly labeled as 61 cm instead of 46 cm. |
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