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GENERATION 5 LINKOW BLADE IMPLANTS

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K822969
510(k) Type
Traditional
Applicant
LEONARD P. LINKOW, D.D.L.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
11/4/1982
Days to Decision
27 days

GENERATION 5 LINKOW BLADE IMPLANTS

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K822969
510(k) Type
Traditional
Applicant
LEONARD P. LINKOW, D.D.L.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
11/4/1982
Days to Decision
27 days