Atlas FDA

ADVANCE TOTAL KNEE SYSTEM

FDA 510(k) clearance K061223 · decided 2006-08-18

Clearance details

K-number
K061223
Device name
ADVANCE TOTAL KNEE SYSTEM
Applicant
Wrightmedicaltechnologyinc
Decision
Substantially Equivalent
Date received
2006-05-02
Decision date
2006-08-18
Days to decision
108 days
Clearance type
Special
Product code
MBH
Device class
2
Regulation number
888.3565
Medical specialty
Orthopedic
Advisory committee
Orthopedic
Location
Arlington, TN, 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
Zimmer® Persona® Personalized Knee System (K251840)Zimmer, Inc.2026-05-28
Persona the Personalized Knee System (Persona Porous Plasma Spray PPS Femurs) (K253189)Zimmer, Inc.2026-03-09
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Balanced Knee System TriMax Porous Femoral Components (K253161)Ortho Development Corp.2025-12-19
Freedom Metaphyseal Cone Implants (Metaphyseal Cones) (K252777)Maxx Orthopedics, Inc.2025-10-31
Triathlon® Total Knee System - Triathlon® Gold Femoral Components (K252044)Howmedica Osteonics Corp., Dba Stryker Orthopaedics2025-10-24
U2 Total Knee System – PF+ Patella; USTAR II System– PF+ Patella (K243656)United Orthopedic Corporation2025-07-31
Physica System (Physica CR Porous Femoral components) (K250980)Lima Corporate S.P.A.2025-05-22
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Recalls involving this device

RecordFirmDate
ADVANCE(R) II MODULAR TIBIAL BASE W/SCREWHOLES, Knee Tibial Base, REF KTTIHA10, SIZE 1 STD recall (Z-2693-2016)MicroPort Orthopedics Inc.2016-09-08
ADVANCE(R) II MODULAR TIBIAL BASE W/SCREWHOLES, Knee Tibial Base, REF KTTIHA11, SIZE 1+; S recall (Z-2694-2016)MicroPort Orthopedics Inc.2016-09-08
ADVANCE(R) II MODULAR TIBIAL BASE W/SCREWHOLES, Knee Tibial Base, REF KTTIHA20, SIZE 2 STD recall (Z-2695-2016)MicroPort Orthopedics Inc.2016-09-08
ADVANCE(R) II MODULAR TIBIAL BASE W/SCREWHOLES, Knee Tibial Base, REF KTTIHA21, SIZE 2+; S recall (Z-2696-2016)MicroPort Orthopedics Inc.2016-09-08
ADVANCE(R) II MODULAR TIBIAL BASE W/SCREWHOLES, Knee Tibial Base, REF KTTIHA30, SIZE 3 STD recall (Z-2697-2016)MicroPort Orthopedics Inc.2016-09-08
ADVANCE(R) II MODULAR TIBIAL BASE W/SCREWHOLES, Knee Tibial Base, REF KTTIHA31, SIZE 3+; S recall (Z-2698-2016)MicroPort Orthopedics Inc.2016-09-08
ADVANCE(R) II MODULAR TIBIAL BASE W/SCREWHOLES, Knee Tibial Base, REF KTTIHA40, SIZE 4 STD recall (Z-2699-2016)MicroPort Orthopedics Inc.2016-09-08
ADVANCE(R) II MODULAR TIBIAL BASE W/SCREWHOLES, Knee Tibial Base, REF KTTIHA41, SIZE 4+; S recall (Z-2700-2016)MicroPort Orthopedics Inc.2016-09-08
ADVANCE(R) II MODULAR TIBIAL BASE W/SCREWHOLES, Knee Tibial Base, REF KTTIHA50, SIZE 5 STD recall (Z-2701-2016)MicroPort Orthopedics Inc.2016-09-08
ADVANCE(R) II MODULAR TIBIAL BASE W/SCREWHOLES, Knee Tibial Base, REF KTTIHA51, SIZE 5+; S recall (Z-2702-2016)MicroPort Orthopedics Inc.2016-09-08
ADVANCE(R) II MODULAR TIBIAL BASE W/SCREWHOLES, Knee Tibial Base, REF KTTIHA60, SIZE 6 STD recall (Z-2703-2016)MicroPort Orthopedics Inc.2016-09-08
ADVANCE (R) CANAL FILLING STEM EXTENSION, REF: KSP1-0140, DIAMETER 11mm, LENGTH 140mm, 1 E recall (Z-0492-2010)Wright Medical Technology Inc2009-12-08
ADVANCE (R) CANAL FILLING STEM EXTENSION, REF: KSP1-2140, DIAMETER 13mm, LENGTH 140mm, 1 E recall (Z-0493-2010)Wright Medical Technology Inc2009-12-08

PMA approvals by this applicant

RecordFirmDate
ADCON(R)-L ADHESION CONTROL IN A BARRIER GEL (P960057/S011)Wrightmedicaltechnologyinc2000-09-27
ADCON-L ADHESION CONTROL IN A BARRIER GEL (P960057/S004)Wrightmedicaltechnologyinc1999-08-11
ADCON-L ADHESION CONTROL IN A BARRIER GEL (P960057/S008)Wrightmedicaltechnologyinc1999-06-02
ADCON-L ADHESION CONTROL IN A BARRIER GEL (P960057/S006)Wrightmedicaltechnologyinc1999-04-21
ADCON-L ADHESION CONTROL IN A BARRIER GEL (P960057/S005)Wrightmedicaltechnologyinc1999-03-18
ADCON -L ADHESION CONTROL IN A BARRIER GEL (P960057/S003)Wrightmedicaltechnologyinc1999-01-14
ADCON -L ADHESION CONTROL IN A BARRIER GEL (P960057/S002)Wrightmedicaltechnologyinc1998-11-25
ADCON-L ANTI-ADHESION CONTROL IN A BARRIER GEL (P960057/S001)Wrightmedicaltechnologyinc1998-09-11