Last synced on 14 June 2024 at 11:05 pm

SYNTHES MINI LENGTHENING APPARATUS

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K973018
510(k) Type
Traditional
Applicant
SYNTHES (USA)
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
11/10/1997
Days to Decision
89 days
Submission Type
Summary

SYNTHES MINI LENGTHENING APPARATUS

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K973018
510(k) Type
Traditional
Applicant
SYNTHES (USA)
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
11/10/1997
Days to Decision
89 days
Submission Type
Summary