FDA 510(k) FDA class 2 Substantially Equivalent 🇳🇱 Netherlands

KURZ SILICONE STRIPS, MODELS SF-1, SF-1W, SF-1 BS

K Number: K033796 · Decision Jan 30, 2004
Classifications
1
FEI Numbers
24
Registration Numbers
24
Same Product Code
32
Applicant Total
14
Review Days
56

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Basic Information

Device Name
KURZ SILICONE STRIPS, MODELS SF-1, SF-1W, SF-1 BS
K Number
K033796
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
874.3620
Medical Specialty
Ear, Nose, Throat
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Heinz Kurz GmbH Medizintechnik
Date Received
December 5, 2003
Decision Date
January 30, 2004
Product Code
KHJ
Advisory Committee
Ear, Nose, Throat
Review Advisory Committee
EN
Third Party
N

Classifications

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

Product Code Device Name
KHJ Polymer, Ent Synthetic-Polyamide (Mesh Or Foil Material)

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Other Clearances by Heinz Kurz GmbH Medizintechnik

K Number Device Name
K130512 NITIFLEX STAPES PROSTHESIS, DETROIT PISTON, SKARZYNSKI PISTON, ROBERSON STAPES PROSTHESIS
K112616 NITIBOND STAPES PROSTHESIS, NITIPLAST STAPES PROSTHESIS
K071150 TROCAR VENTILATION TUBE/WITH TROCAR TIP, TROCAR HANDLE, MODEL 1015 074, 1015 076, 1015 075, 1015 077, W/ RETENTION WIRE
K042503 KURZ CLIP PISTON MVP, MODEL 1006 711-13/0.4 MM + 1006 761-63/0.6MM
K021479 CLIP PISTON AWENGEN, MODEL# 1006 805 - 1006 861
K013573 CLIP PARTIAL PROSTHESIS-TITANIUM DRESDEN, MODEL 1002 250-257
K011115 KURZ UPPER EYELID IMPLANT- PLATINUM/IRIDIUM,MODELS REGULAR 4007 003-007, SPECIAL 4007 002, 4007 008-010
K002221 KURKZ K-PISTON TITANIUM STAPEDIAL PROSTHESIS, MODEL 1006 103-1006 170
K001123 KURZ UPPER EYELID IMPLANT SIZERS, MODEL 8000 111
K000127 KURZ PURE GOLD UPPER EYELIDS IMPLANT (OBERASCHER), MODEL 4001 02-4001 10
Search all 14 clearances from Heinz Kurz GmbH Medizintechnik →