Last synced on 14 November 2025 at 11:06 pm

EXPLOR MODULAR RADIAL HEAD REPLACEMENT DEVICE

Page Type
Cleared 510(K)
510(k) Number
K051385
510(k) Type
Traditional
Applicant
Biomet, Inc.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
8/5/2005
Days to Decision
70 days
Submission Type
Summary

EXPLOR MODULAR RADIAL HEAD REPLACEMENT DEVICE

Page Type
Cleared 510(K)
510(k) Number
K051385
510(k) Type
Traditional
Applicant
Biomet, Inc.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
8/5/2005
Days to Decision
70 days
Submission Type
Summary