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

NORMED TITANIUM MINIPLATE SYSTEM

K Number: K931539 · Decision Jul 5, 1994
Classifications
1
FEI Numbers
106
Registration Numbers
106
Same Product Code
291
Applicant Total
9
Review Days
463

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Basic Information

Device Name
NORMED TITANIUM MINIPLATE SYSTEM
K Number
K931539
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
872.4760
Medical Specialty
Dental
Decision
Substantially Equivalent
Statement or Summary
Statement
Applicant
Normed Medizin-Technik GmbH
Date Received
March 29, 1993
Decision Date
July 5, 1994
Product Code
JEY
Advisory Committee
Dental
Review Advisory Committee
DE
Third Party
N

Classifications

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

Product Code Device Name
JEY Plate, Bone

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Other Clearances by Normed Medizin-Technik GmbH

K Number Device Name
K151708 RECON system - Compression Screws
K151701 Tenodesis screw system
K152256 RECON system- Grubber Lapidus-, Platar Lapidus-, Tarsalis Plates and Screws
K152312 RECON system-V-TEK-IVP Plates and Screws
K152142 RECON system - MPJ-Plates
K151407 RECON system
K133035 NORMED PELLEGRIN CALCANEUS STOP SCREW
K123347 NORMED ANKLE FIX SYSTEM 4.0 AND NORMED ANKLE FIX PLUS SYSTEM 4.0