Last synced on 14 November 2025 at 11:06 pm

MJS POSTERIOR STABILIZED KNEE SYSTEM

Page Type
Cleared 510(K)
510(k) Number
K012762
510(k) Type
Traditional
Applicant
OSTEOIMPLANT TECHNOLOGY, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
12/11/2001
Days to Decision
116 days
Submission Type
Statement

MJS POSTERIOR STABILIZED KNEE SYSTEM

Page Type
Cleared 510(K)
510(k) Number
K012762
510(k) Type
Traditional
Applicant
OSTEOIMPLANT TECHNOLOGY, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
12/11/2001
Days to Decision
116 days
Submission Type
Statement