FDA 510(k) FDA unclassified Substantially Equivalent 🇺🇸 United States

PRIMATRIX AG ANTIMICROBIAL DERMAL DERMAL REPAIR SCAFFOLD

K Number: K100261 · Decision Dec 10, 2010
Classifications
1
FEI Numbers
384
Registration Numbers
385
Same Product Code
702
Applicant Total
16
Review Days
316

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
PRIMATRIX AG ANTIMICROBIAL DERMAL DERMAL REPAIR SCAFFOLD
K Number
K100261
Device Class
FDA unclassified
Clearance Type
Abbreviated
Medical Specialty
Unknown
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Tei Biosciences, Inc.
Date Received
January 28, 2010
Decision Date
December 10, 2010
Product Code
FRO
Advisory Committee
Unknown
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
FRO Dressing, Wound, Drug

Similar 510(k) Clearances

Other 510(k) clearances with the same product code (FRO), 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
K083898 SURGIMEND
K083440 PRIMATRIX DERMAL REPAIR SCAFFOLD
K071807 ORTHOMEND SOFT TISSUE MATRIX
K061407 PRIMATRIX DERMAL REPAIR SCAFFOLD
K060829 COSMATRIX
K060984 XENFORM SOFT TISSUE REPAIR MATRIX
K060989 TISSUEMEND SOFT TISSUE REPAIR MATRIX
Search all 16 clearances from Tei Biosciences, Inc. →