NUVASIVE MASH


Device Classification Name

spinal vertebral body replacement device

510(k) Number K023319
Device Name NUVASIVE MASH
Original Applicant
NUVASIVE, INC.
10065 old grove rd.
san diego, 
CA 
92131

Original Contact laetitia bernard
Regulation Number 888.3060
Classification Product Code
MQP  
Date Received 10/04/2002
Decision Date 03/04/2003
Decision

substantially equivalent

(SESE)

Regulation Medical Specialty

Orthopedic

510k Review Panel

Orthopedic

summary

summary

Type Traditional
Reviewed by Third Party No

Combination Product

No