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N/A 23067

by Medtronic PS Medical United States GUDID

Product code LKG

Regulatory status

as of 24 Oct 2026

RegionAuthorizationNumberDateStatus
United StatesGUDID listing Number00763000029630 UDI-DIDate8 Mar 2020ListedStatusIn distribution

Coverage

1 jurisdiction

United States of AmericaUnited States of AmericaUnited States of AmericaUnited States of AmericaUnited States of AmericaUnited States of AmericaUnited States of AmericaUnited States of AmericaUnited States of AmericaUnited States of AmericaUnited States of AmericaUnited States of AmericaUnited States of AmericaUnited States of AmericaUnited States of AmericaUnited States of AmericaUnited States of AmericaUnited States of AmericaUnited States of AmericaUnited States of AmericaUnited States of AmericaUnited States of AmericaUnited States of AmericaUnited States of AmericaUnited States of AmericaUnited States of AmericaUnited States of AmericaUnited States of AmericaUnited States of AmericaUnited States of AmericaUnited States of AmericaUnited States of AmericaUnited States of AmericaUnited States of AmericaUnited States of AmericaUnited States of AmericaUnited States of AmericaUnited States of AmericaUnited States of AmericaUnited States of AmericaUnited States of AmericaUnited States of AmericaUnited States of AmericaUnited States of AmericaUnited States of AmericaUnited States of AmericaUnited States of AmericaUnited States of AmericaUnited States of AmericaUnited States of AmericaUnited States of AmericaUnited States of AmericaUnited States of AmericaUnited States of AmericaUnited States of AmericaUnited States of AmericaUnited States of AmericaUnited States of AmericaUnited States of AmericaUnited States of AmericaUnited States of AmericaUnited States of AmericaUnited States of AmericaUnited States of AmericaUnited States of AmericaUnited States of AmericaUnited States of AmericaUnited States of AmericaUnited States of AmericaUnited States of AmericaUnited States of AmericaUnited States of AmericaUnited States of AmericaUnited States of AmericaUnited States of AmericaUnited States of AmericaUnited States of AmericaUnited States of AmericaUnited States of AmericaUnited States of AmericaUnited States of AmericaUnited States of AmericaUnited States of AmericaUnited States of AmericaUnited States of AmericaUnited States of AmericaUnited States of AmericaUnited States of AmericaUnited States of AmericaUnited States of AmericaUnited States of America
  • Listed
  • Not covered

United States — GUDID listing Listed

Recalls

29 recalls · FDA

  • 29 recalls, same reason

    • Terminated Z-1146-2009 FDA Unclassified (pre-2012) initiated 12 Feb 2009 via K874498, on the same 510(k)
    • Terminated Z-1128-2009 FDA Unclassified (pre-2012) initiated 12 Feb 2009 via K874498, on the same 510(k)
    • Terminated Z-1150-2009 FDA Unclassified (pre-2012) initiated 12 Feb 2009 via K874498, on the same 510(k)
    • Terminated Z-1132-2009 FDA Unclassified (pre-2012) initiated 12 Feb 2009 via K874498, on the same 510(k)
    • Terminated Z-1124-2009 FDA Unclassified (pre-2012) initiated 12 Feb 2009 via K874498, on the same 510(k)
    • Terminated Z-1151-2009 FDA Unclassified (pre-2012) initiated 12 Feb 2009 via K874498, on the same 510(k)
    • Terminated Z-1129-2009 FDA Unclassified (pre-2012) initiated 12 Feb 2009 via K874498, on the same 510(k)
    • Terminated Z-1149-2009 FDA Unclassified (pre-2012) initiated 12 Feb 2009 via K874498, on the same 510(k)
    • Terminated Z-1131-2009 FDA Unclassified (pre-2012) initiated 12 Feb 2009 via K874498, on the same 510(k)
    • Terminated Z-1126-2009 FDA Unclassified (pre-2012) initiated 12 Feb 2009 via K874498, on the same 510(k)
    • Terminated Z-1135-2009 FDA Unclassified (pre-2012) initiated 12 Feb 2009 via K874498, on the same 510(k)
    • Terminated Z-1137-2009 FDA Unclassified (pre-2012) initiated 12 Feb 2009 via K874498, on the same 510(k)
    • Terminated Z-1125-2009 FDA Unclassified (pre-2012) initiated 12 Feb 2009 via K874498, on the same 510(k)
    • Terminated Z-1139-2009 FDA Unclassified (pre-2012) initiated 12 Feb 2009 via K874498, on the same 510(k)
    • Terminated Z-1142-2009 FDA Unclassified (pre-2012) initiated 12 Feb 2009 via K874498, on the same 510(k)
    • Terminated Z-1148-2009 FDA Unclassified (pre-2012) initiated 12 Feb 2009 via K874498, on the same 510(k)
    • Terminated Z-1144-2009 FDA Unclassified (pre-2012) initiated 12 Feb 2009 via K874498, on the same 510(k)
    • Terminated Z-1134-2009 FDA Unclassified (pre-2012) initiated 12 Feb 2009 via K874498, on the same 510(k)
    • Terminated Z-1127-2009 FDA Unclassified (pre-2012) initiated 12 Feb 2009 via K874498, on the same 510(k)
    • Terminated Z-1143-2009 FDA Unclassified (pre-2012) initiated 12 Feb 2009 via K874498, on the same 510(k)
    • Terminated Z-1147-2009 FDA Unclassified (pre-2012) initiated 12 Feb 2009 via K874498, on the same 510(k)
    • Terminated Z-1145-2009 FDA Unclassified (pre-2012) initiated 12 Feb 2009 via K874498, on the same 510(k)
    • Terminated Z-1141-2009 FDA Unclassified (pre-2012) initiated 12 Feb 2009 via K874498, on the same 510(k)
    • Terminated Z-1136-2009 FDA Unclassified (pre-2012) initiated 12 Feb 2009 via K874498, on the same 510(k)
    • Terminated Z-1140-2009 FDA Unclassified (pre-2012) initiated 12 Feb 2009 via K874498, on the same 510(k)
    • Terminated Z-1138-2009 FDA Unclassified (pre-2012) initiated 12 Feb 2009 via K874498, on the same 510(k)
    • Terminated Z-1130-2009 FDA Unclassified (pre-2012) initiated 12 Feb 2009 via K874498, on the same 510(k)
    • Terminated Z-1133-2009 FDA Unclassified (pre-2012) initiated 12 Feb 2009 via K874498, on the same 510(k)
    • Terminated Z-1152-2009 FDA Unclassified (pre-2012) initiated 12 Feb 2009 via K874498, on the same 510(k)

    The ventricular catheters may become detached from the Snap Base assembly after implantation and this condition may increase the need for emergency revision surgery.

Recalls marked "via" name another device cleared under the same FDA submission as this one.

Specification

GUDID · synced 23 Oct 2026

Trade Name
N/A
Generic Name
Cerebrospinal fluid shunt adaptor
Model / Reference
23067
Primary DI / UDI-DI
00763000029630
510(k) Number
FDA Product Code
LKG
GMDN Term
Cerebrospinal fluid shunt adaptor
Device Class
Class II
Regulation Number
882.5550
Commercial Distribution
In Commercial Distribution

Related devices

Category: Cerebrospinal fluid shunt adaptor

Cleared under the same submission (K874498)

Show all (12)

Similar devices

Also classified as Cerebrospinal fluid shunt adaptor.

Other devices from Medtronic PS Medical

See all devices from Medtronic PS Medical →

Properties & raw data

Show properties, registry sources and raw records
  • Sterile
  • Single Use
  • Prescription Use
  • Lot / Batch Number
Other properties (10)
  • Implantable: No
  • Contains Latex: No
  • Over-the-Counter: No
  • Convenience Kit: No
  • Combination Product: No
  • HCT/P: No
  • Premarket Exempt: No
  • Serial Number: No
  • Expiration Date: No
  • Manufacturing Date: No

Sources (1)

  • FDA UDI 6aa42333-c9f1-48ce-a3b2-fb45d46a5a48 35 fields · synced 23 Oct 2026