Atlas FDA

UNIVERSAL TOTAL WRIST SYSTEM (MODIFICATION)

FDA 510(k) clearance K961051 · decided 1996-06-06

Clearance details

K-number
K961051
Device name
UNIVERSAL TOTAL WRIST SYSTEM (MODIFICATION)
Applicant
Kinetikos Medical, Inc.
Decision
Substantially Equivalent
Date received
1996-03-11
Decision date
1996-06-06
Days to decision
87 days
Clearance type
Traditional
Product code
JWJ
Device class
2
Regulation number
888.3800
Medical specialty
Orthopedic
Advisory committee
Orthopedic
Location
San Diego, CA, US
Third-party review
No
Expedited review
No

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RecordFirmDate
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Arthrosurface WristMotion Total Wrist Arthroplasty System (K200718)Arthrosurface, Inc.2020-10-15
KinematX Total Wrist Arthroplasty System (K191525)Extremity Medical, LLC2020-03-04
INTEGRA FREEDOM WRIST ARTHROPLASTY SYSTEM (K132250)Integra LifeSciences Corporation2014-03-24
MAESTRO WRIST FRACTURE IMPLANT (K080426)Biomet Manufacturing Corp2008-07-29
MAESTRO TOTAL WRIST (K042032)Biomet, Inc.2004-10-07
BIAX A.F. WRIST/BIAX ADVANCED FIXATION WRIST (K031203)DePuy Orthopaedics, Inc.2003-07-14
UNIVERSAL TOTAL WRIST SYSTEM (K030037)Kinetikos Medical, Inc.2003-02-05
WRIST IMPLANT (K021859)Avanta Orthopaedics, Inc.2002-12-02
MODIFICATION TO UNIVERSAL TOTAL WRIST SYSTEM (K020554)Kinetikos Medical, Inc.2002-05-03

Recalls involving this device

No recalls on record reference this clearance.