Last synced on 30 May 2025 at 11:05 pm

SPINALPLANE

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K934336
510(k) Type
Traditional
Applicant
SYNVASIVE TECHNOLOGY, INC.
Country
United States
FDA Decision
Substantially Equivalent for Some Indications
Decision Date
3/10/1995
Days to Decision
549 days
Submission Type
Summary

SPINALPLANE

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K934336
510(k) Type
Traditional
Applicant
SYNVASIVE TECHNOLOGY, INC.
Country
United States
FDA Decision
Substantially Equivalent for Some Indications
Decision Date
3/10/1995
Days to Decision
549 days
Submission Type
Summary