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

UCR SPINAL SYSTEM

K Number: K032739 · Decision Nov 20, 2003
Classifications
1
FEI Numbers
342
Registration Numbers
342
Same Product Code
302
Applicant Total
5
Review Days
77

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
UCR SPINAL SYSTEM
K Number
K032739
Device Class
FDA class 2
Clearance Type
Special
Regulation Number
888.3070
Medical Specialty
Orthopedic
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Seaspine
Date Received
September 4, 2003
Decision Date
November 20, 2003
Product Code
MNI
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
MNI Orthosis, Spinal Pedicle Fixation

Similar 510(k) Clearances

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

View all

Other Clearances by Seaspine

K Number Device Name
K043232 UCR SPINAL SYSTEM
K040130 ANTERIOR LUMBAR BUTTRESS SYSTEM
K032368 SONOMA ANTERIOR CERVICAL PLATE SYSTEM
K031381 UCR SPINAL SYSTEM, LAMINAR HOOKS, PEDICLE HOOKS, AND INSTRUMENTS