Last synced on 14 November 2025 at 11:06 pm

Mg OSTEOINJECT™; Mg OSTEOREVIVE™; Mg OSTEOCRETE™

Page Type
Cleared 510(K)
510(k) Number
K234013
510(k) Type
Traditional
Applicant
Bone Solutions, Inc.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
2/5/2024
Days to Decision
48 days
Submission Type
Summary

Mg OSTEOINJECT™; Mg OSTEOREVIVE™; Mg OSTEOCRETE™

Page Type
Cleared 510(K)
510(k) Number
K234013
510(k) Type
Traditional
Applicant
Bone Solutions, Inc.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
2/5/2024
Days to Decision
48 days
Submission Type
Summary