FDA 510(k) FDA unclassified Substantially Equivalent 🇺🇸 United States

SPARTAN S3 FACET SYSTEM

K Number: K092568 · Decision Nov 17, 2009
Classifications
1
FEI Numbers
100
Registration Numbers
100
Same Product Code
77
Applicant Total
16
Review Days
89

Research this 510(k) in seconds

The Research Assistant summarizes clearance history, predicates and product-code trends — and cites every record.

Free to try · every answer cites its records

Basic Information

Device Name
SPARTAN S3 FACET SYSTEM
K Number
K092568
Device Class
FDA unclassified
Clearance Type
Traditional
Medical Specialty
Unknown
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Amendia, Inc.
Date Received
August 20, 2009
Decision Date
November 17, 2009
Product Code
MRW
Advisory Committee
Unknown
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
MRW System, Facet Screw Spinal Device

Similar 510(k) Clearances

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

View all

Other Clearances by Amendia, Inc.

K Number Device Name
K160924 Amendia Interbody Fusion Devices
K161842 Overwatch Spine System
K152920 Savannah-T® Pedicle Screw System
K153152 Syzygy Stabilization System
K160291 Optimus ALIF System
K152972 Amendia Stand-Alone Cervical System
K151310 Amendia Interbody Fusion Devices
K152460 Rectangular Corpectomy Cage
K152455 Amendia Cervical Plate System
K151322 Amendia Interbody Fusion Devices
Search all 16 clearances from Amendia, Inc. →