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CAMLOG SCREW IMPLANT SYSTEM

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K000099
510(k) Type
Special
Applicant
ALTATEC BIOTECHNOLOGIES
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
1/28/2000
Days to Decision
15 days
Submission Type
Statement

CAMLOG SCREW IMPLANT SYSTEM

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K000099
510(k) Type
Special
Applicant
ALTATEC BIOTECHNOLOGIES
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
1/28/2000
Days to Decision
15 days
Submission Type
Statement