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

MODIFICATION TO DEPUY DELTA XTEND REVERSE SHOULDER SYSTEM

K Number: K081620 · Decision Jun 30, 2008
Classifications
1
FEI Numbers
218
Registration Numbers
218
Same Product Code
189
Applicant Total
207
Review Days
21

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Basic Information

Device Name
MODIFICATION TO DEPUY DELTA XTEND REVERSE SHOULDER SYSTEM
K Number
K081620
Device Class
FDA class 2
Clearance Type
Special
Regulation Number
888.3660
Medical Specialty
Orthopedic
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
DePuy Orthopaedics, Inc.
Date Received
June 9, 2008
Decision Date
June 30, 2008
Product Code
KWS
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
KWS Prosthesis, Shoulder, Semi-Constrained, Metal/Polymer Cemented

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Other Clearances by DePuy Orthopaedics, Inc.

K Number Device Name
K252887 DePuy ATTUNE™ Knee System
K231503 CUPTIMIZE™ Advanced
K213839 DePuy Corail AMT Hip Prosthesis
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
Search all 207 clearances from DePuy Orthopaedics, Inc. →