Atlas FDA

INTEGRA ARTIFICIAL SKIN

FDA premarket approval P900033/S003 · decided 1999-11-23

Approval details

PMA number
P900033
Supplement
S003
Supplement type
30-Day Notice
Supplement reason
Process Change - Manufacturer/Sterilizer/Packager/Supplier
Trade name
INTEGRA ARTIFICIAL SKIN
Generic name
Dressing, wound and burn, interactive
Applicant
Integra Lifesciences Corp.
Date received
1999-11-08
Decision date
1999-11-23
Days to decision
15 days
Decision code
OK30
Product code
MGR
Advisory committee
General, Plastic Surgery
Expedited review
No
Location
Plainsboro, NJ
Statement
The 30-Day Notice requested a change to the Quality Control test used to determine the chondroitin-6-sulfate content in INTEGRA(R) Artificial Skin, Dermal Regeneration Template.

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
Codman Disposable Perforators (K183581)Integra Lifesciences Corp.2019-01-20
CereLink ICP Monitor, CereLink ICP Extension Cable (K183406)Integra Lifesciences Corp.2019-01-11
CodMan Certas Plus Programmable Valve (K182265)Integra Lifesciences Corp.2018-11-20
Codman Certas Plus Electronic Tool Kit (K181902)Integra Lifesciences Corp.2018-10-25
CUSA Excel+ (K150682)Integra Lifesciences Corp.2015-12-18
Integra (R) Jarit (R) Kerrison Rongeurs, Integra (R) Ruggles (TM)-Redmons (TM) Kerrison Rongeurs, Integra (R) Miltex (R) Kerrison Rongeurs, Integra (R) Meisterhand (R) Kerrison Rongeurs (K150428)Integra Lifesciences Corp.2015-04-16
INTEGRA LICOX PTO2 MONITOR (K131184)Integra Lifesciences Corp.2013-08-30
JARIT, RUGGLES, R&B REDMOND/ REDMOND, MILTEX, MEISTERHAND - KERRISON RONGEURS (K092227)Integra Lifesciences Corp.2010-02-17