Atlas FDA

COLLAGEN RIBBON

FDA 510(k) clearance K120019 · decided 2012-02-23

Clearance details

K-number
K120019
Device name
COLLAGEN RIBBON
Applicant
Wrightmedicaltechnologyinc
Decision
Substantially Equivalent
Date received
2012-01-03
Decision date
2012-02-23
Days to decision
51 days
Clearance type
Traditional
Product code
FTM
Device class
2
Regulation number
878.3300
Medical specialty
General, Plastic Surgery
Advisory committee
General, Plastic Surgery
Location
Arlington, TN, US
Third-party review
No
Expedited review
No

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Recalls involving this device

No recalls on record reference this clearance.

PMA approvals by this applicant

RecordFirmDate
ADCON(R)-L ADHESION CONTROL IN A BARRIER GEL (P960057/S011)Wrightmedicaltechnologyinc2000-09-27
ADCON-L ADHESION CONTROL IN A BARRIER GEL (P960057/S004)Wrightmedicaltechnologyinc1999-08-11
ADCON-L ADHESION CONTROL IN A BARRIER GEL (P960057/S008)Wrightmedicaltechnologyinc1999-06-02
ADCON-L ADHESION CONTROL IN A BARRIER GEL (P960057/S006)Wrightmedicaltechnologyinc1999-04-21
ADCON-L ADHESION CONTROL IN A BARRIER GEL (P960057/S005)Wrightmedicaltechnologyinc1999-03-18
ADCON -L ADHESION CONTROL IN A BARRIER GEL (P960057/S003)Wrightmedicaltechnologyinc1999-01-14
ADCON -L ADHESION CONTROL IN A BARRIER GEL (P960057/S002)Wrightmedicaltechnologyinc1998-11-25
ADCON-L ANTI-ADHESION CONTROL IN A BARRIER GEL (P960057/S001)Wrightmedicaltechnologyinc1998-09-11