510(k) K953881

SPINE SYSTEM SACRAL PLATE by J.B.S., S.A. — Product Code MNH

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)

Source: FDA 510(k) database entry for K953881. Report a data issue: hello@regdatalab.com.