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FDA 510(k)

MANAN SPRITACRE SPINAL NEEDLES

K-Number: K011209 · 2001-06-26

ApplicantManan Medical Products, Inc.
Decision Date2001-06-26
Product CodeBSP
Advisory CommitteeAN
DecisionSubstantially Equivalent

Device Summary

MANAN SPRITACRE SPINAL NEEDLES is the device name listed in this FDA 510(k) record. The listed applicant is Manan Medical Products, Inc.. It received FDA 510(k) clearance on 2001-06-26 under 510(k) number K011209. The device is classified under product code BSP. It was reviewed by the AN advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the MANAN SPRITACRE SPINAL NEEDLES?

MANAN SPRITACRE SPINAL NEEDLES is a medical device that received FDA 510(k) clearance on 2001-06-26. The listed applicant is Manan Medical Products, Inc.. The 510(k) number is K011209.

When did MANAN SPRITACRE SPINAL NEEDLES receive FDA 510(k) clearance?

MANAN SPRITACRE SPINAL NEEDLES received FDA 510(k) clearance on 2001-06-26, under 510(k) number K011209.

Who is the listed applicant for MANAN SPRITACRE SPINAL NEEDLES?

The FDA 510(k) record lists Manan Medical Products, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for MANAN SPRITACRE SPINAL NEEDLES?

The FDA product code for MANAN SPRITACRE SPINAL NEEDLES is BSP.

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Other records listing Manan Medical Products, Inc. as applicant

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Related Devices (Code: BSP)

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

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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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