Atlas FDA

FPC/SFPC/RFPC ACETABULAR COMPONENT

FDA 510(k) clearance K915529 · decided 1993-07-13

Clearance details

K-number
K915529
Device name
FPC/SFPC/RFPC ACETABULAR COMPONENT
Applicant
Implantology Corp.
Decision
Substantially Equivalent
Date received
1991-12-10
Decision date
1993-07-13
Days to decision
581 days
Clearance type
Traditional
Product code
JDL
Device class
3
Regulation number
888.3320
Medical specialty
Orthopedic
Advisory committee
Orthopedic
Location
Pine Brook, NJ, 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
VERSYS EPOCH FULLCOAT HIP PROSTHESIS, MODEL 4088 SERIES (K073499)Zimmer, Inc.2008-08-07
DYNASTY ACETABULAR SYSTEM (K070785)Wrightmedicaltechnologyinc2007-07-11
DYNASTY ACETABULAR SHELL AND COCR ACETABULAR LINER (K061844)Wrightmedicaltechnologyinc2006-12-06
PROFEMUR RENAISSANCE HIP STEM (K051995)Wrightmedicaltechnologyinc2005-08-22
CONSERVE TOTAL FEMORAL HEAD (K051348)Wrightmedicaltechnologyinc2005-08-19
M2A/C2A ACETABULAR SYSTEM (K042841)Biomet, Inc.2004-12-21
PROFEMUR S HIP STEM (K041586)Wrightmedicaltechnologyinc2004-07-09
PROFEMUR TAPERED HIP STEM (K041114)Wrightmedicaltechnologyinc2004-05-28
METAL TRANSCEND ARTICULATION SYSTEM (K004043)Wrightmedicaltechnologyinc2001-07-13
METAL BACKED ACETABULAR COMPONENT (K950542)Encore Orthopedics, Inc.1995-05-25
P.F.C. APICAL PLUG (K944769)Johnson & Johnson Professionals, Inc.1994-12-08
ACETABULAR DOME HOLE PLUGS (K942809)Osteonics Corp.1994-09-20

Recalls involving this device

No recalls on record reference this clearance.