EBI SPF IMPLANTABLE SPINAL FUSION STIMULATOR
FDA premarket approval P850035/S032 · decided 2008-08-15
Approval details
- PMA number
- P850035
- Supplement
- S032
- Supplement type
- 30-Day Notice
- Supplement reason
- Process Change - Manufacturer/Sterilizer/Packager/Supplier
- Trade name
- EBI SPF IMPLANTABLE SPINAL FUSION STIMULATOR
- Generic name
- Stimulator, invasive bone growth
- Applicant
- Ahp Eos Buyer, Inc.
- Date received
- 2008-07-17
- Decision date
- 2008-08-15
- Days to decision
- 29 days
- Decision code
- OK30
- Product code
- LOE
- Advisory committee
- Orthopedic
- Expedited review
- No
- Location
- Parsippany, NJ
- Statement
- ADDITION OF A CONFORMAL COATING ADHESIVE TO THE ELECTRONIC PRINTED CIRCUIT BOARDS OF THE DEVICE.
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