Scotts Surgical Retractor and Elastic
FDA 510(k) K791665 · Lone Star Medical Products, Inc.
510(k) numberK791665
Submission
- Device name
- Scotts Surgical Retractor and Elastic
- Applicant
- Lone Star Medical Products, Inc.
Mchenry, IL, US - Received
- August 21, 1979
- Decision date
- September 19, 1979
- Decision
- Substantially Equivalent (SESE)
- Type
- Traditional 510(k)
Device classification
- Product code
- GAD – Retractor
- Device class
- Class I (low risk)
- Regulation
- 21 CFR 878.4800
- Specialty
- General, Plastic Surgery
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| K152538 | JRP Wound SpreaderGAD · Traditional | J.R. Parker, LLC | 04/13/2016SE |
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| K132645 | Thoratrak Mics Retractor System, Rack, BladesGAD · Traditional | Medtronic, Inc. | 10/04/2013SE |
| K071775 | DashGAD · Traditional | Ezsurgical | 08/07/2007SE |
| K050256 | Apple Medical/Ob Mobius Elastic RetractorGAD · Traditional | Apple Medical Corp. | 04/26/2005SE |
| K043602 | Quadrant Retractor SystemGAD · Traditional | Medtronic Sofamor Danek | 02/23/2005SE |
| K001339 | MRI Fastsystem Retractor SystemGAD · Special | Omni-Tract Surgical, Div. Minn. Scientific, Inc. | 05/17/2000SE |
| K980588 | Clarus Endoscopic Discectomy System Sitetrac Model 6000GAD · Traditional | Clarus Medical Systems, Inc. | 08/18/1998SE |
| K963006 | Scion Saphenous Vein Harvesting SystemGAD · Traditional | Scion International, Inc. | 09/20/1996SE |
| K943875 | Villalta RetractorGAD · Traditional | Hct, Inc. | 11/09/1994SE |
More from Hct, Inc.
| 510(k) | Device | Decision |
|---|---|---|
| K850041 | P-3 Closing Instrument · Traditional | 02/21/1985SE |
| K831531 | Surgical Isolation Barrier System · Traditional | 06/05/1984SE |
| K820015 | Urethal Cutter ClampKOA · Traditional | 02/22/1982SE |
| K810915 | The Scott DialmenzensertKOA · Traditional | 05/08/1981SE |
| K802983 | The Inquinal Resorvoir InserterKOA · Traditional | 12/30/1980SE |
Questions and answers
When was Scotts Surgical Retractor and Elastic cleared by the FDA?
Scotts Surgical Retractor and Elastic (K791665) received a 510(k) decision of Substantially Equivalent on September 19, 1979, 29 days after the submission was received.
What is the product code of K791665?
The FDA product code is GAD – Retractor, a Class I (low risk) device regulated under 21 CFR 878.4800.