Last synced on 14 November 2025 at 11:06 pm

ANTERIOR CRUCIATE LIGAMENT (ACL) INSTRUMENT SYSTEM

Page Type
Cleared 510(K)
510(k) Number
K011102
510(k) Type
Traditional
Applicant
AESCULAP, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
8/3/2001
Days to Decision
114 days
Submission Type
Summary

ANTERIOR CRUCIATE LIGAMENT (ACL) INSTRUMENT SYSTEM

Page Type
Cleared 510(K)
510(k) Number
K011102
510(k) Type
Traditional
Applicant
AESCULAP, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
8/3/2001
Days to Decision
114 days
Submission Type
Summary