FDA 510(k) FDA class 2 Substantially Equivalent 🇺🇸 United States

COSMATRIX

K Number: K060829 · Decision May 17, 2006
Classifications
1
FEI Numbers
89
Registration Numbers
89
Same Product Code
162
Applicant Total
16
Review Days
51

Research this 510(k) in seconds

The Research Assistant summarizes clearance history, predicates and product-code trends — and cites every record.

Free to try · every answer cites its records

Basic Information

Device Name
COSMATRIX
K Number
K060829
Device Class
FDA class 2
Clearance Type
Abbreviated
Regulation Number
878.3300
Medical Specialty
General, Plastic Surgery
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Tei Biosciences, Inc.
Date Received
March 27, 2006
Decision Date
May 17, 2006
Product Code
FTM
Advisory Committee
General, Plastic Surgery
Review Advisory Committee
SU
Third Party
N

Classifications

This FDA 510(k) entry is associated with 1 FDA classification via its product code.

Product Code Device Name
FTM Mesh, Surgical

Similar 510(k) Clearances

Other 510(k) clearances with the same product code (FTM), ordered by most recent decision date.

View all

Other Clearances by Tei Biosciences, Inc.

K Number Device Name
K162965 SurgiMend MP Collagen Matrix for Soft Tissue Reconstruction
K153690 PriMatrix Dermal Repair Scaffold
K131286 PRIMATRIX DERMAL REPAIR SCAFFOLD
K100261 PRIMATRIX AG ANTIMICROBIAL DERMAL DERMAL REPAIR SCAFFOLD
K083898 SURGIMEND
K083440 PRIMATRIX DERMAL REPAIR SCAFFOLD
K071807 ORTHOMEND SOFT TISSUE MATRIX
K061407 PRIMATRIX DERMAL REPAIR SCAFFOLD
K060984 XENFORM SOFT TISSUE REPAIR MATRIX
K060989 TISSUEMEND SOFT TISSUE REPAIR MATRIX
Search all 16 clearances from Tei Biosciences, Inc. →