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FEMORAL & TIBIAL AUGMENT BLOCK

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K924940
510(k) Type
Traditional
Applicant
JOINT MEDICAL PRODUCTS CORP.
Country
United States
FDA Decision
Substantially Equivalent for Some Indications
Decision Date
3/9/1993
Days to Decision
160 days
Submission Type
Statement

FEMORAL & TIBIAL AUGMENT BLOCK

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K924940
510(k) Type
Traditional
Applicant
JOINT MEDICAL PRODUCTS CORP.
Country
United States
FDA Decision
Substantially Equivalent for Some Indications
Decision Date
3/9/1993
Days to Decision
160 days
Submission Type
Statement