PMA P900033S013

Device
INTEGRA DERMAL REGENERATION TEMPLATE
Applicant
Integra Lifesciences Corp.
PMA number
P900033
Supplement
S013
Product code
MDD
Decision date
2005-12-29
Classification
Device, Dermal Replacement
Generic name
Device, dermal replacement
Approval order statement
MANUFACTURING EQUIPMENT CHANGE.

Current openFDA PMA Record#

Device
INTEGRA DERMAL REGENERATION TEMPLATE
Applicant
Integra Lifesciences Corp.
PMA number
P900033
Supplement
S013
Product code
MDD
Generic name
Device, dermal replacement
Decision date
2005-12-29
Decision code
OK30
Date received
2005-12-06
Supplement type
30-Day Notice
Supplement reason
Process Change - Manufacturer/Sterilizer/Packager/Supplier
Approval order statement
MANUFACTURING EQUIPMENT CHANGE.