510(k) K953881
K953881 is an FDA 510(k) premarket notification submitted by J.B.S., S.A. for the device "SPINE SYSTEM SACRAL PLATE". The FDA issued a decision of Substantially Equivalent for Some Indications on Feb 21, 1996. The device falls under product code MNH (Orthosis, Spondylolisthesis Spinal Fixation), a Class II device regulated under 21 CFR 888.3070. J.B.S., S.A. has 9 other 510(k) clearances on record.
Clearance Details
- Decision
- SN (Substantially Equivalent for Some Indications)
- Decision Date
- Feb 21, 1996
- Date Received
- Aug 18, 1995
- Clearance Type
- Traditional
- Expedited Review
- No
- Third Party Review
- No
Device Classification
- Device Name
- Orthosis, Spondylolisthesis Spinal Fixation
- Device Class
- Class II
- Regulation Number
- 888.3070
- Review Panel
- OR
- Submission Type
- 510(k)