510(k) K222270 · ODP Intervertebral Fusion Device With Bone Graft, Cervical

HEDRON Cervical Spacers, HEDRON Lumbar Spacers, SABLE Expandable Spacer, ExcelsiusGPS Instruments

Applicant	Globus Medical, Inc., Audubon PA, US
Decision	Substantially Equivalent, Oct 21, 2022
Received	Jul 29, 2022
Type	Traditional
FDA record	Open on fda.gov

Recalls that name K222270

No recall in the FDA data names this 510(k).

Links come from the 510(k) numbers listed on each FDA recall record. We don't infer predicate chains.