The following data is part of a premarket notification filed by Howmedica Corp. with the FDA for Pca(r) Modular Total Knee Tib Insert Durocon Baseplate.
Device ID | K940861 |
510k Number | K940861 |
Device Name: | PCA(R) MODULAR TOTAL KNEE TIB INSERT DUROCON BASEPLATE |
Classification | Prosthesis, Knee, Patellofemorotibial, Semi-constrained, Cemented, Polymer/metal/polymer |
Applicant | HOWMEDICA CORP. 359 VETERANS BLVD. Rutherford, NJ 07070 |
Contact | Robert E Smith |
Correspondent | Robert E Smith HOWMEDICA CORP. 359 VETERANS BLVD. Rutherford, NJ 07070 |
Product Code | JWH |
CFR Regulation Number | 888.3560 [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Traditional |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 1994-02-23 |
Decision Date | 1995-09-18 |