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PSI FLEXIBLE ARM

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K942601
510(k) Type
Traditional
Applicant
V. MUELLER NEURO/SPINE
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
12/27/1994
Days to Decision
209 days
Submission Type
Statement