Last synced on 17 May 2024 at 11:06 pm

CUTTER, P606 BONE

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K770302
510(k) Type
Traditional
Applicant
DENTRONIX INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
3/9/1977
Days to Decision
21 days

CUTTER, P606 BONE

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K770302
510(k) Type
Traditional
Applicant
DENTRONIX INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
3/9/1977
Days to Decision
21 days