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

DEPUY MOTECH MOSS MIAMI SPINAL SYSTEM

K Number: K982011 · Decision Aug 6, 1998
Classifications
1
FEI Numbers
321
Registration Numbers
321
Same Product Code
429
Applicant Total
207
Review Days
59

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Basic Information

Device Name
DEPUY MOTECH MOSS MIAMI SPINAL SYSTEM
K Number
K982011
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
888.3050
Medical Specialty
Orthopedic
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
DePuy Orthopaedics, Inc.
Date Received
June 8, 1998
Decision Date
August 6, 1998
Product Code
KWP
Advisory Committee
Orthopedic
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
KWP Appliance, Fixation, Spinal Interlaminal

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K210167 DELTA XTEND Reverse Shoulder System
K203167 DePuy Corail AMT Hip Prosthesis
K202472 ACTIS Duofix Hip Prosthesis
K201347 DePuy ATTUNE™ Total Knee System
K193540 TRUMATCH Personalized Solutions
K193398 Summit DuoFix HA Coating
K192946 DePuy Corail AMT Hip Prosthesis
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