Last synced on 21 June 2024 at 11:04 pm

SPY Laparoscope

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K221217
510(k) Type
Traditional
Applicant
Stryker
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
6/17/2022
Days to Decision
51 days
Submission Type
Summary