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Recall Observatory FDA recall evidence

Device product

Kelyniam Custom Skull Implant (CSI), Model no. PEEK-IM1001 (Small)

Z-1870-2018

June 10, 2017

Class II

Product summary

Firm
Kelyniam Global, Inc.
Event
Event 79791
Status
Terminated
Classification
Class II
Quantity
2
Official record key
device-enforcement:Z-1870-2018

Official wording

Reason: Significant design changes made to the Custom Skull Implant (CSI) devices, such as removing pressure relief holes across the length of the device and adding suture holes along the ridge of the implant, were not validated or submitted to FDA for marketing clearance. The Temporal Suture System (TSS) is no longer being offered and the Integrated Fixation System (IFS) has been temporarily suspended

Code information: Marketing Material: All revisions up to rev. A. IFU: All revisions up to rev. C. Case Numbers: CSI041216-CM1 CSI092016-LD1L

Distribution pattern: US nationwide distribution.

Derived failure modes

  • Unknown

    reason.no_named_rule · v1.0.0

    Significant design changes made to the Custom Skull Implant (CSI) devices, such as removing pressure relief holes across the length of the device and adding suture holes along the ridge of the implant, were not validated or submitted to FDA for marketing clearance. The Temporal Suture System (TSS) is no longer being offered and the Integrated Fixation System (IFS) has been temporarily suspended