Surgical Retractor
FDA 510(k) K760422 · Cutter Laboratories, Inc.
510(k) numberK760422
Submission
- Device name
- Surgical Retractor
- Applicant
- Cutter Laboratories, Inc.
Mchenry, IL, US - Received
- August 10, 1976
- Decision date
- August 23, 1976
- 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 |
| K151104 | Otelo LLGAD · Traditional | Spineart | 01/06/2016SE |
| 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 |
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|---|---|---|
| K861315 | Hyperbaric Penetration Extension SetCBF · Traditional | 05/21/1986SE |
| K854106 | BaysilexELW · Traditional | 03/17/1986SE |
| K842324 | PerfourmELW · Traditional | 11/09/1984SE |
| K834106 | Intravenous Infusion ControllerLDR · Traditional | 05/30/1984SE |
| K832237 | Orthopedic Casting Tape MaxcastITG · Traditional | 08/16/1983SE |
| K823214 | Dosimetric Release Program - Admin. SetFPA · Traditional | 01/12/1983SE |
| K821326 | Cutter Bond Polycarboxylate CementEMA · Traditional | 05/28/1982SE |
| K813532 | Cutterbond Zinc Phosphate CementEMA · Traditional | 03/02/1982SE |
| K802105 | C-BladeHWE · Traditional | 09/16/1980SE |
| K802104 | C-SplintIQI · Traditional | 09/16/1980SE |
Questions and answers
When was Surgical Retractor cleared by the FDA?
Surgical Retractor (K760422) received a 510(k) decision of Substantially Equivalent on August 23, 1976, 13 days after the submission was received.
What is the product code of K760422?
The FDA product code is GAD – Retractor, a Class I (low risk) device regulated under 21 CFR 878.4800.