Tendon Leader
FDA 510(k) K853764 · Orthopedic Systems, Inc.
510(k) numberK853764
Submission
- Device name
- Tendon Leader
- Applicant
- Orthopedic Systems, Inc.
Hayward, CA, US - Received
- September 9, 1985
- Decision date
- October 7, 1985
- Decision
- Substantially Equivalent (SESE)
- Type
- Traditional 510(k)
Device classification
No product code recorded.
More from Orthopedic Systems, Inc.
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|---|---|---|
| K952495 | Anchors Away Soft Tissue Attachment SystemLXH · Traditional | 01/22/1996SE |
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| K910736 | Jackson Multipurpose Operating TableJEA · Traditional | 05/21/1991SE |
| K910031 | Park City Shoulder PositionerFWZ · Traditional | 01/24/1991SE |
| K903938 | C Fit CupJDI · Traditional | 01/04/1991SN |
| K892503 | Nuffield Total KneeJWH · Traditional | 05/04/1990SN |
| K896678 | Silicone PlugHRX · Traditional | 01/30/1990SE |
| K894283 | Comprehensive Spine Motion AnalyzerKQX · Traditional | 01/19/1990SE |
| K890498 | Freeman Modular Hip Stem Ridged VersionJDI · Traditional | 10/13/1989SN |
| K890331 | Freeman Total Hip System Ridged StemLWJ · Traditional | 10/13/1989SE |
Questions and answers
When was Tendon Leader cleared by the FDA?
Tendon Leader (K853764) received a 510(k) decision of Substantially Equivalent on October 7, 1985, 28 days after the submission was received.