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

GalaFLEX LITE Scaffold

K Number: K233999 · Decision Apr 9, 2024
Classifications
1
FEI Numbers
12
Registration Numbers
12
Same Product Code
12
Applicant Total
18
Review Days
113

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
GalaFLEX LITE Scaffold
K Number
K233999
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
Tepha, Inc.
Date Received
December 18, 2023
Decision Date
April 9, 2024
Product Code
OOD
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
OOD Surgical Film

Similar 510(k) Clearances

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

View all

Other Clearances by Tepha, Inc.

K Number Device Name
K202425 SurgiLattice scaffold
K211307 GalaSTITCH Absorbable Monofilament Suture
K162922 GalaFORM 3D
K161092 GalaSHAPE 3D
K140533 GALAFLEX MESH
K132348 TEPHAFLEX BRAIDED SUTURE
K130326 TEPHAFLEX MELTBLOWN CONSTRUCT
K113721 TEPHAFLEX LIGHT MESH
K113723 TEPHAFLEX MESH
K111946 TEPHAFLEX MESH
Search all 18 clearances from Tepha, Inc. →