Side Cutting Serrated Blade

FDA 510(k) K841980 · Stainless Mfg., Inc.

Substantially Equivalent

510(k) numberK841980

Submission

Device name
Side Cutting Serrated Blade
Applicant
Stainless Mfg., Inc.
Mchenry, IL, US
Received
May 14, 1984
Decision date
August 15, 1984
Decision
Substantially Equivalent (SESE)
Type
Traditional 510(k)

Official FDA 510(k) record

Device classification

Product code
HTZ – Instrument, Cutting, Orthopedic
Device class
Class I (low risk)
Regulation
21 CFR 878.4800
Specialty
General, Plastic Surgery

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K842111Kogan Endospeculum 9-1/2HTZ · Traditional J. Sklar Mfg. Co., Inc.06/19/1984SE
K841982Meniscotome 4MM & 5MMHTZ · Traditional Stainless Mfg., Inc.06/19/1984SE
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More from Stainless Mfg., Inc.

510(k)DeviceDecision
K841982Meniscotome 4MM & 5MMHTZ · Traditional 06/19/1984SE
K8419814MM & 5MM FileHTP · Traditional 06/19/1984SE
K8419794MM Cup CurretteHTF · Traditional 06/19/1984SE
K841978Lateral Release Knife 5MM & 7MMHTZ · Traditional 06/19/1984SE
K8419775MM Dougle Edge Ring CuretteHTZ · Traditional 06/19/1984SE
K841976Hook Knife 4MM & 5MMHTZ · Traditional 06/19/1984SE
K841975Rosette Knife 4MMHTZ · Traditional 06/19/1984SE
K841974Retrograde Knife 4MM & 5MMHTZ · Traditional 06/19/1984SE
K841973Banana Knife SerratedHTZ · Traditional 06/19/1984SE
K841972Banana Knife - K841969-LABELINGHTZ · Traditional 06/19/1984SE

Questions and answers

When was Side Cutting Serrated Blade cleared by the FDA?

Side Cutting Serrated Blade (K841980) received a 510(k) decision of Substantially Equivalent on August 15, 1984, 93 days after the submission was received.

What is the product code of K841980?

The FDA product code is HTZ – Instrument, Cutting, Orthopedic, a Class I (low risk) device regulated under 21 CFR 878.4800.