510(k) K060989

TISSUEMEND SOFT TISSUE REPAIR MATRIX by Tei Biosciences, Inc. — Product Code FTM

K060989 is an FDA 510(k) premarket notification submitted by Tei Biosciences, Inc. for the device "TISSUEMEND SOFT TISSUE REPAIR MATRIX". The FDA issued a decision of Substantially Equivalent on May 15, 2006. The device falls under product code FTM (Mesh, Surgical), a Class II device regulated under 21 CFR 878.3300. Tei Biosciences, Inc. has at least 10 other 510(k) clearances on record.

Clearance Details

Decision
SESE (Substantially Equivalent)
Decision Date
May 15, 2006
Date Received
April 10, 2006
Clearance Type
Special
Expedited Review
No
Third Party Review
No

Device Classification

Device Name
Mesh, Surgical
Device Class
Class II
Regulation Number
878.3300
Review Panel
SU
Submission Type