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

STRYKER SPINE MAPS SYSTEM

K Number: K032855 · Decision Dec 10, 2003
Classifications
1
FEI Numbers
326
Registration Numbers
326
Same Product Code
308
Applicant Total
13
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
STRYKER SPINE MAPS SYSTEM
K Number
K032855
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
888.3070
Medical Specialty
Orthopedic
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Howmedica Osteonics
Date Received
September 12, 2003
Decision Date
December 10, 2003
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.

View all

Other Clearances by Howmedica Osteonics

K Number Device Name
K120578 ACCOLADE II HIP STEM
K102019 RESTORATION ACETABULAR WEDGE AUGMENTS
K063423 TRIATHLON CS (CONDYLAR STABILIZING) LIPPED INSERT
K033258 BONESAVE BONE VOID FILLER
K031702 REFLEX ANTERIOR CERVICAL PLATE SYSTEM
K031435 BONESOURCE BVF
K031217 GMRS PRESS FIT STEMS WITH PUREFIX HA
K022461 S2 FEMORAL NAIL
K022160 XIA SPINAL SYSTEM
K013772 MODIFICATION TO HOFFMANN II MICRO EXTERNAL FIXATION SYSTEM
Search all 13 clearances from Howmedica Osteonics →