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FDA 510(k)

Meril-Bonewax

K-Number: K200452 · 2023-03-27

ApplicantM/s. Meril Endo Surgery Private Limited.
Decision Date2023-03-27
Product CodeMTJ
DecisionSubstantially Equivalent

Device Summary

Meril-Bonewax is a medical device manufactured by M/s. Meril Endo Surgery Private Limited.. It received FDA 510(k) clearance on 2023-03-27 under approval number K200452. The device is classified under product code MTJ. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the Meril-Bonewax?

Meril-Bonewax is a medical device that received FDA 510(k) clearance on 2023-03-27. It is manufactured by M/s. Meril Endo Surgery Private Limited.. The 510(k) number is K200452.

When was Meril-Bonewax approved by the FDA?

Meril-Bonewax received FDA 510(k) clearance on 2023-03-27, under approval number K200452.

What company makes Meril-Bonewax?

Meril-Bonewax is manufactured by M/s. Meril Endo Surgery Private Limited..

What is the FDA product code for Meril-Bonewax?

The FDA product code for Meril-Bonewax is MTJ.

Other Devices by M/s. Meril Endo Surgery Private Limited.

K160623FILASILK - Natural Non-absorbable Silk Surgical Suture, FILAMIDE - Non Absorbable polyamide surgical Sutures, MERICRON XL - Non Absorbable Polyester Surgical Suture, FILAPROP - Non Absorbable Polypropylene surgical Suture K172149FILASILK - Natural Non-absorbable Silk Surgical Suture, FILAMIDE - Non Absorbable polyamide surgical Sutures, MERICRON XL - Non Absorbable Polyester Surgical Suture, FILAPROP - Non Absorbable Polypropylene surgical Suture K172659MEGASORB - Natural absorbable Polyglycolic Acid Surgical Suture, MITSU - Absorbable Polyglactin 910 Surgical Sutures, MITSU FST - Absorbable Polyglactin 910 Surgical Suture, FILAXYN - Absorbable Polydioxanone Surgical (PDS), FILAPRON - Absorbable poly(glycolide-co-caprolactone) Surgical Suture K172146MERISTEEL K200166Mirus Ligating Clip, Mirus Ligating Clip Applier K200320Mirus Circular Stapler, Mirus Linear Cutter and Reload, Mirus Hemorrhoidal Circular Stapler, Mirus Linear Stapler and Reload

View all 11 devices →

Related Devices (Code: MTJ)

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Official Source

View on FDA Database →

Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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