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

VIPER F2 FACET FIXATION SYSTEM

K Number: K101762 · Decision Nov 15, 2010
Classifications
1
FEI Numbers
100
Registration Numbers
100
Same Product Code
77
Applicant Total
68
Review Days
146

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
VIPER F2 FACET FIXATION SYSTEM
K Number
K101762
Device Class
FDA unclassified
Clearance Type
Special
Medical Specialty
Unknown
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Depuy Spine, Inc.
Date Received
June 22, 2010
Decision Date
November 15, 2010
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 Depuy Spine, Inc.

K Number Device Name
K201831 CONFIDENCE Spinal Cement System
K142185 EXPEDIUM VERSE SPINE SYSTEM
K111136 EXPEDIUM SPINE SYSTEM, VIPER SYSTEM, VIPER 2 SYSTEM
K121020 VIPER SYSTEM
K110353 MOUNTAINEER OCT SPINAL SYSTEM
K110216 EXPEDIUM SYSTEM, VIPER SYSTEM
K103133 VEPER SYSTEM, EXPEDIUM SYSTEM
K101993 VIPER SYSTEM, EXPEDIUM SYSTEM
K103100 MOUNTAINEER OCT SPINAL SYSTEM
K102701 VIPER SPINE SYSTEM
Search all 68 clearances from Depuy Spine, Inc. →