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ENDOSCOPIC MORTONS NEUROMA INSTRUMENTS

Page Type
Cleared 510(K)
510(k) Number
K940230
510(k) Type
Traditional
Applicant
INSTRATEK, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
12/12/1994
Days to Decision
332 days
Submission Type
Statement

ENDOSCOPIC MORTONS NEUROMA INSTRUMENTS

Page Type
Cleared 510(K)
510(k) Number
K940230
510(k) Type
Traditional
Applicant
INSTRATEK, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
12/12/1994
Days to Decision
332 days
Submission Type
Statement