510(k) K073530
K073530 is an FDA 510(k) premarket notification submitted by Accelerated Innovation, LLC for the device "ACCIN ANTERIOR CERVICAL PLATE SYSTEM". The FDA issued a decision of Substantially Equivalent on January 31, 2008. The device falls under product code KWQ (Appliance, Fixation, Spinal Intervertebral Body), a Class II device regulated under 21 CFR 888.3060. Accelerated Innovation, LLC has at least 6 other 510(k) clearances on record.
Clearance Details
- Decision
- SESE (Substantially Equivalent)
- Decision Date
- January 31, 2008
- Date Received
- December 17, 2007
- Clearance Type
- Traditional
- Expedited Review
- No
- Third Party Review
- No
Device Classification
- Device Name
- Appliance, Fixation, Spinal Intervertebral Body
- Device Class
- Class II
- Regulation Number
- 888.3060
- Review Panel
- OR
- Submission Type