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

MTF FASCIA

K Number: K120479 · Decision Nov 8, 2012
Classifications
1
FEI Numbers
32
Registration Numbers
32
Same Product Code
13
Applicant Total
24
Review Days
266

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Basic Information

Device Name
MTF FASCIA
K Number
K120479
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
878.3300
Medical Specialty
General, Plastic Surgery
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Musculoskeletal Transplant Foundation
Date Received
February 16, 2012
Decision Date
November 8, 2012
Product Code
OWY
Advisory Committee
General, Plastic Surgery
Review Advisory Committee
OR
Third Party
N

Classifications

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

Product Code Device Name
OWY Mesh, Surgical, Collagen, Orthopaedics, Reinforcement Of Tendon

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Other Clearances by Musculoskeletal Transplant Foundation

K Number Device Name
K181633 MTF Pre-Sutured Tendon
K121313 MTF NEW BONE VOID FILLER
K113167 MTF NEW BONE VOILD FILLER
K110003 MTF NEW BONE VOID FILLER
K103795 DBX DEMINERALIZED BONE MATRIX PUTTY
K103784 DBX DEMINERALIZED BONE MATRIX PUTTY
K091217 DBX DEMINERALIZED BONE MATRIX PUTTY
K091218 DBX DEMINERALIZED BONE MATRIX PUTTY
K080399 DBX DEMINERALIZED BONE MATRIX PUTTY, DBX DEMINERALIZED BONE MATRIX PASTE
K080405 SYGNAL DBM
Search all 24 clearances from Musculoskeletal Transplant Foundation →