The following data is part of a premarket notification filed by Wright Medical Technology, Inc. with the FDA for Ortholoc Advantim Ps Lsi Tibial Insert.
Device ID | K940235 |
510k Number | K940235 |
Device Name: | ORTHOLOC ADVANTIM PS LSI TIBIAL INSERT |
Classification | Prosthesis, Knee, Patellofemorotibial, Semi-constrained, Cemented, Polymer/metal/polymer |
Applicant | WRIGHT MEDICAL TECHNOLOGY, INC. 5677 AIRLINE RD. Arlington, TN 38002 |
Contact | Judy English |
Correspondent | Judy English WRIGHT MEDICAL TECHNOLOGY, INC. 5677 AIRLINE RD. Arlington, TN 38002 |
Product Code | JWH |
CFR Regulation Number | 888.3560 [🔎] |
Decision | Substantially Equivalent For Some Indications (SN) |
Type | Traditional |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 1994-01-18 |
Decision Date | 1994-10-05 |