FDA applicant
Spinal Specialties, Inc.
FDA records 8 decisions for Spinal Specialties, Inc. (San Antonio, TX) from 1994 to 1996: 8 510(k) clearances. Most are in product codes CAZ (Anesthesia Conduction Kit) and BSP (Needle, Conduction, Anesthetic (W/Wo Introducer)). 2 recalls are linked to its devices.
Data to Oct 25, 2026 (FDA decisions) Oct 12, 2026 (recalls) refreshed weekly
How often FDA has decided Spinal Specialties, Inc.’s devices, and how often a recall has named them.
FDA decisions per year
No FDA decision for Spinal Specialties, Inc. since 2007.
Recalls per year
2in 2016
Class I Class II/III not classified
Planning a device like Spinal Specialties, Inc.’s? A 510(k) Report ranks candidate predicates for your device by lineage, citations and recall history, with the review-time outlook.
See the 510(k) ReportOther applicant names beginning “Spinal”
FDA records each applicant name separately; these may or may not be the same firm.