510(k) K032473 ยท HRX Arthroscope
DEKOMPRESSOR PERCUTANEOUS DISCECTOMY PROBE
| Applicant | Stryker Instruments, Kalamazoo MI, US |
| Decision | Substantially Equivalent, Nov 7, 2003 |
| Received | Aug 12, 2003 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K032473
| Date | Firm and product | Code | Linked 510(k) |
|---|---|---|---|
| Nov 1, 2013 | Stryker Instruments Div. of Stryker Corporation Dekompressor Percutaneous Discectomy Probe.
The Dekompressor is a single use disposable discectomy probe that passes through and works in conjunction with an introducer cannula to remove intervertebr Terminated |
HRX | None listed |
| Mar 28, 2011 | Stryker Instruments Division of Stryker Corporation Interventional Pain 6" 13 G (2.4 mm) Percutaneous Discectomy Probe, REF 407-265, Sterile, Stryker Instruments, Kalamazoo, MI.
The DeKompressor Percutaneous Discectomy Probe is intended for use in th Terminated |
HRX | None listed |
| Mar 28, 2011 | Stryker Instruments Division of Stryker Corporation Interventional Pain 6" 15 G (1.85 mm) Percutaneous Discectomy Probe, REF 407-266, Sterile, Stryker Instruments, Kalamazoo, MI.
The DeKompressor Percutaneous Discectomy Probe is intended for use in t Terminated |
HRX | None listed |
Links come from the 510(k) numbers listed on each FDA recall record. We don't infer predicate chains.