Last synced on 14 November 2025 at 11:06 pm

RESURFACE PROSHESIS

Page Type
Cleared 510(K)
510(k) Number
K781343
510(k) Type
Traditional
Applicant
AESCULAP INSTRUMENTS CORP.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
9/27/1978
Days to Decision
54 days

RESURFACE PROSHESIS

Page Type
Cleared 510(K)
510(k) Number
K781343
510(k) Type
Traditional
Applicant
AESCULAP INSTRUMENTS CORP.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
9/27/1978
Days to Decision
54 days