Atlas FDA

LUMBAR I/F CAGE SYSTEM

FDA premarket approval P960025/S010 · decided 2004-03-17

Approval details

PMA number
P960025
Supplement
S010
Supplement type
Normal 180 Day Track
Supplement reason
Location Change - Manufacturer/Sterilizer/Packager/Supplier
Trade name
LUMBAR I/F CAGE SYSTEM
Generic name
SPINAL PEDICLE SCREW, FIXATION, APPLIANCE SYSTEM
Applicant
Depuy Spine, Inc.
Date received
2003-02-24
Decision date
2004-03-17
Days to decision
387 days
Decision code
APPR
Product code
MCV
Advisory committee
Orthopedic
Expedited review
No
Location
Raynham, MA
Statement
APPROVAL FOR A MANUFACTURING SITE LOCATED AT DEPUY ACROMED SARL, LELOCLE, SWITZERLAND.

Class III intelligence, same tools

PMAs share the API, exports and alerts with 510(k) data - watch an applicant and hear about every approval.

510(k) clearances by this applicant

RecordFirmDate
CONFIDENCE Spinal Cement System (K201831)Depuy Spine, Inc.2020-08-31
EXPEDIUM VERSE SPINE SYSTEM (K142185)Depuy Spine, Inc.2014-11-19
EXPEDIUM SPINE SYSTEM, VIPER SYSTEM, VIPER 2 SYSTEM (K111136)Depuy Spine, Inc.2012-06-14
VIPER SYSTEM (K121020)Depuy Spine, Inc.2012-05-03
MOUNTAINEER OCT SPINAL SYSTEM (K110353)Depuy Spine, Inc.2011-04-07
EXPEDIUM SYSTEM, VIPER SYSTEM (K110216)Depuy Spine, Inc.2011-04-01
VEPER SYSTEM, EXPEDIUM SYSTEM (K103133)Depuy Spine, Inc.2011-01-18
VIPER SYSTEM, EXPEDIUM SYSTEM (K101993)Depuy Spine, Inc.2010-12-07