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MOD. PERCUTANEOUS ARTHROSCOPIC MICRO DISCECTOMY

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K922519
510(k) Type
Traditional
Applicant
SMITH & NEPHEW, INC.
Country
United States
FDA Decision
Substantially Equivalent for Some Indications
Decision Date
3/29/1994
Days to Decision
685 days
Submission Type
Statement

MOD. PERCUTANEOUS ARTHROSCOPIC MICRO DISCECTOMY

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K922519
510(k) Type
Traditional
Applicant
SMITH & NEPHEW, INC.
Country
United States
FDA Decision
Substantially Equivalent for Some Indications
Decision Date
3/29/1994
Days to Decision
685 days
Submission Type
Statement