Last synced on 23 May 2025 at 11:06 pm

SYNTHES (USA) [SYNTHES] MINI EXTERNAL FIXATOR

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K971987
510(k) Type
Traditional
Applicant
SYNTHES (USA)
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
6/24/1997
Days to Decision
26 days
Submission Type
Statement

SYNTHES (USA) [SYNTHES] MINI EXTERNAL FIXATOR

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K971987
510(k) Type
Traditional
Applicant
SYNTHES (USA)
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
6/24/1997
Days to Decision
26 days
Submission Type
Statement