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WASHERLOC SCREW SYSTEM, LIGAMENT SCREW SYSTEM, NO-PROFILE BI-CORTICAL SCREW SYSTEM, CHANNEL LIGAMENT CLAMP, HECKMAN SCRE

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K981967
510(k) Type
Traditional
Applicant
ARTHROTEK/BIOMET, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
7/17/1998
Days to Decision
43 days
Submission Type
Summary

WASHERLOC SCREW SYSTEM, LIGAMENT SCREW SYSTEM, NO-PROFILE BI-CORTICAL SCREW SYSTEM, CHANNEL LIGAMENT CLAMP, HECKMAN SCRE

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K981967
510(k) Type
Traditional
Applicant
ARTHROTEK/BIOMET, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
7/17/1998
Days to Decision
43 days
Submission Type
Summary