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FDA 510(k)

SCHULTZ MP COMPONENT PUNCH

K-Number: K870846 · 1987-03-13

Decision Date1987-03-13
Product CodeHWP
Advisory CommitteeOR
DecisionSubstantially Equivalent

Device Summary

SCHULTZ MP COMPONENT PUNCH is the device name listed in this FDA 510(k) record. The listed applicant is Warsaw Orthopedic, Inc.. It received FDA 510(k) clearance on 1987-03-13 under 510(k) number K870846. The device is classified under product code HWP. It was reviewed by the OR advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the SCHULTZ MP COMPONENT PUNCH?

SCHULTZ MP COMPONENT PUNCH is a medical device that received FDA 510(k) clearance on 1987-03-13. The listed applicant is Warsaw Orthopedic, Inc.. The 510(k) number is K870846.

When did SCHULTZ MP COMPONENT PUNCH receive FDA 510(k) clearance?

SCHULTZ MP COMPONENT PUNCH received FDA 510(k) clearance on 1987-03-13, under 510(k) number K870846.

Who is the listed applicant for SCHULTZ MP COMPONENT PUNCH?

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

What is the FDA product code for SCHULTZ MP COMPONENT PUNCH?

The FDA product code for SCHULTZ MP COMPONENT PUNCH is HWP.

Related Clinical Trials

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.

Other records listing Warsaw Orthopedic, Inc. as applicant

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

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

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