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FDA 510(k)

Vista BC Putty

K-Number: K241457 · 2024-08-28

ApplicantInter-Med, Inc.
Decision Date2024-08-28
Product CodeKIF
Advisory CommitteeDE
DecisionSubstantially Equivalent

Device Summary

Vista BC Putty is a medical device manufactured by Inter-Med, Inc.. It received FDA 510(k) clearance on 2024-08-28 under approval number K241457. The device is classified under product code KIF. It was reviewed by the DE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the Vista BC Putty?

Vista BC Putty is a medical device that received FDA 510(k) clearance on 2024-08-28. It is manufactured by Inter-Med, Inc.. The 510(k) number is K241457.

When was Vista BC Putty approved by the FDA?

Vista BC Putty received FDA 510(k) clearance on 2024-08-28, under approval number K241457.

What company makes Vista BC Putty?

Vista BC Putty is manufactured by Inter-Med, Inc..

What is the FDA product code for Vista BC Putty?

The FDA product code for Vista BC Putty is KIF.

Other Devices by Inter-Med, Inc.

K211721PS System K221811Vista BC Sealer K241354Sealer Solvent K241489ReminGel K253337REGEN Bioactive Cement

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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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