Atlas FDA

DISTAL RADIO-ULNAR JOINT IMPLANT

FDA 510(k) clearance K082839 · decided 2008-10-24

Clearance details

K-number
K082839
Device name
DISTAL RADIO-ULNAR JOINT IMPLANT
Applicant
Aptis Medical, LLC
Decision
Substantially Equivalent
Date received
2008-09-26
Decision date
2008-10-24
Days to decision
28 days
Clearance type
Special
Product code
KXE
Device class
2
Regulation number
888.3810
Medical specialty
Orthopedic
Advisory committee
Orthopedic
Location
Glenview, KY, US
Third-party review
No
Expedited review
No

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Similar devices under this product code

Devices cleared under the same product code - the starting set for predicate research.

RecordFirmDate
Aptis Medical Distal Radio Ulnar Joint Implant (K190599)Aptis Medical, LLC2019-05-03
Aptis Medical Distal Radio Ulnar Joint Implant (K142569)Aptis Medical, LLC2015-04-03
FIRST CHOICE DRUJ SYSTEM, PARTIAL HEAD IMPLANT (K112481)Ascension Orthopedic2012-04-09
ISOELASTICU (K081025)Remi Sciences, Inc.2008-11-21
SBI ULNAR HEAD IMPLANT (K061146)Small Bone Innovations, Inc.2006-07-19
DISTAL RADIO-ULNAR JOINT IMPLANT (K053119)Aptis Medical, LLC2005-12-07
ASCENSION MUH (K052137)Ascension Orthopedics, Inc.2005-11-03
DISTAL RADIO-ULNAR JOINT IMPLANT (K040497)Aptis Medical, LLC2005-01-26
HERBERT ULNAR HEAD PROSTHESIS SYSTEM (K042902)Stuckenbrock Medizintechnik GmbH2004-12-27
KAPP CUSTOM ULNAR HEAD WRIST IMPLANT (K033930)Kapp Surgical Instrument, Inc.2004-07-28
WMT MODULAR ULNAR HEAD IMPLANT (K020274)Wrightmedicaltechnologyinc2002-02-22
ULNAR HEAD IMPLANT (K010786)Avanta Orthopaedics, Inc.2001-04-11

Recalls involving this device

No recalls on record reference this clearance.