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Instrument, Shunt System Implantation
FDA product code GYK · Class 1 · Neurology
58
Registered devices
15
Adverse events
1
Recalls
13
510(k) clearances
Devices with this code
AESCULAP — Aesculap AGSubcutaneous Guidewire - Medium — ARKIS BIOSCIENCES INC.Single Pass Tunneling Guidewire - Small — ARKIS BIOSCIENCES INC.Precision Tunneler - Medium — ARKIS BIOSCIENCES INC.CODMAN — Cerenovus, Inc.AESCULAP — Aesculap AGPhoenix Neuro — SOPHYSAAESCULAP — Aesculap AGCODMAN® — INTEGRA LIFESCIENCES PRODUCTION CORPORATIONN/A — MEDTRONIC PS MEDICAL, INC.AESCULAP — Aesculap AGCODMAN® — INTEGRA LIFESCIENCES PRODUCTION CORPORATIONNatus® — NATUS MEDICAL INCORPORATEDSophysa — SOPHYSACODMAN® — INTEGRA LIFESCIENCES PRODUCTION CORPORATIONIntegra® — Integra Lifesciences CorporationCODMAN — Cerenovus, Inc.AESCULAP — Aesculap AGNatus® — NATUS MEDICAL INCORPORATEDNatus® — NATUS MEDICAL INCORPORATEDSubcutaneous Guidewire - Large — ARKIS BIOSCIENCES INC.Integra® — INTEGRA NEUROSCIENCES IMPLANT (FRANCE)Natus® — NATUS MEDICAL INCORPORATEDNatus® — NATUS MEDICAL INCORPORATED
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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