Last synced on 14 November 2025 at 11:06 pm

CEMENT AND BONE REMOVAL KIT

Page Type
Cleared 510(K)
510(k) Number
K961759
510(k) Type
Traditional
Applicant
MAILLEFER INSTRUMENTS S.A.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
6/13/1996
Days to Decision
37 days
Submission Type
Statement

CEMENT AND BONE REMOVAL KIT

Page Type
Cleared 510(K)
510(k) Number
K961759
510(k) Type
Traditional
Applicant
MAILLEFER INSTRUMENTS S.A.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
6/13/1996
Days to Decision
37 days
Submission Type
Statement