Last synced on 25 January 2026 at 3:41 am

ACTIVELOCK MODULAR FEMORAL HIP SYSTEM

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K980020
510(k) Type
Traditional
Applicant
Metagen, LLC
Country
United States
FDA Decision
Substantially Equivalent for Some Indications
Decision Date
4/3/1998
Days to Decision
88 days

ACTIVELOCK MODULAR FEMORAL HIP SYSTEM

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K980020
510(k) Type
Traditional
Applicant
Metagen, LLC
Country
United States
FDA Decision
Substantially Equivalent for Some Indications
Decision Date
4/3/1998
Days to Decision
88 days