Last synced on 14 November 2025 at 11:06 pm

ARTHREX INSTRUMENTS (WRIST)

Page Type
Cleared 510(K)
510(k) Number
K926303
510(k) Type
Traditional
Applicant
ARTHREX, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
1/26/1994
Days to Decision
407 days
Submission Type
Statement

ARTHREX INSTRUMENTS (WRIST)

Page Type
Cleared 510(K)
510(k) Number
K926303
510(k) Type
Traditional
Applicant
ARTHREX, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
1/26/1994
Days to Decision
407 days
Submission Type
Statement