FDA-Device2024-10-02Class II
AVS Anchor-C Cervical Cage System Instructions For Use (IFU)- eIFU (revision 5)-Indicated for anterior cervical interbody fusion procedures in skeletally mature patients with cervical disc disease at one level from the C2-C3 disc to the C7-T1 disc.
Stryker Spine
Hazard
Labeling Correction: Instructions For Use (IFU)-Updated electronic Rev 5, specific language for indications for use for the United States and Canada was inadvertently removed.
Sold states
Worldwide distribution - US Nationwide and the country of Canada.
Affected count
8,589 units
Manufactured in
2 Pearl Ct, Allendale, NJ, United States
Products
AVS Anchor-C Cervical Cage System Instructions For Use (IFU)- eIFU (revision 5)-Indicated for anterior cervical interbody fusion procedures in skeletally mature patients with cervical disc disease at one level from the C2-C3 disc to the C7-T1 disc.
Official notice
https://www.accessdata.fda.gov/scripts/ires/index.cfm?Product=Z-3210-2024Don't want to check this manually?
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