FDA 510(k) FDA class 2 Substantially Equivalent for Some Indications 🇺🇸 United States

SPINE SYSTEM SACRAL PLATE

K Number: K953881 · Decision Feb 21, 1996
Classifications
1
FEI Numbers
326
Registration Numbers
326
Same Product Code
308
Applicant Total
10
Review Days
187

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Basic Information

Device Name
SPINE SYSTEM SACRAL PLATE
K Number
K953881
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
888.3070
Medical Specialty
Orthopedic
Decision
Substantially Equivalent for Some Indications
Applicant
J.B.S., S.A.
Date Received
August 18, 1995
Decision Date
February 21, 1996
Product Code
MNH
Advisory Committee
Orthopedic
Review Advisory Committee
OR
Third Party
N

Classifications

This FDA 510(k) entry is associated with 1 FDA classification via its product code.

Product Code Device Name
MNH Orthosis, Spondylolisthesis Spinal Fixation

Similar 510(k) Clearances

Other 510(k) clearances with the same product code (MNH), ordered by most recent decision date.

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Other Clearances by J.B.S., S.A.

K Number Device Name
K962757 J.B.S. SPINE SYSTEM WITH PEDICLE SCREWS - ADDITIONAL COMPONENTS - SCREWS, LINKING PLATES, HOOKS AND ROD CLAMP
K955864 J.B. S. C1-C2 CLAMP
K953599 CLAMP ASSEMBLY
K952298 SPINAL PEDICLE SCREW, FIXATION, APPLIANCE
K942432 J.B.S. CERVICAL SPINE SYSTEM
K940666 JBS SMOOTH FIXATION PIN
K940669 J.B.S. B.A.C. PIN
K940673 J.B.S. SELF-TAPPING THREADED PIN
K935113 J.B.S. IMPLANTABLE SPINAL FIXATION DEVICE