FDA 510(k) FDA class 2 Unknown 🇺🇸 United States

RABEA DEVICE, MODEL PXXXXXX

K Number: K990345 · Decision Jul 30, 1999
Classifications
1
FEI Numbers
23
Registration Numbers
23
Same Product Code
53
Applicant Total
23
Review Days
176

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Basic Information

Device Name
RABEA DEVICE, MODEL PXXXXXX
K Number
K990345
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
878.3300
Medical Specialty
General, Plastic Surgery
Decision
Unknown
Statement or Summary
Summary
Applicant
Signus Medizintechnik GmbH
Date Received
February 4, 1999
Decision Date
July 30, 1999
Product Code
JDK
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
JDK Prosthesis, Hip, Cement Restrictor

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K212755 SIGNUS SACRONAIL® Transsacral Stabilization System
K151704 Diplomat® Spinal System
K141405 MOBIS II ST SPINAL IMPLANT
K123758 TASMIN R
K131372 MOBIS II
K122317 TETRIS II
K111792 MOBIS, MOVAL, SEMIAL, TETRISMODEL PEEK AND TITANIUM, KIMBA MODEL STANDARD AND MINI
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