SCHULTZ PROSTHESIS COMPONENT INSERTER EXTRACTOR
K-Number: K870844 · 1987-03-13
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Device Summary
Frequently Asked Questions
What is the SCHULTZ PROSTHESIS COMPONENT INSERTER EXTRACTOR?
SCHULTZ PROSTHESIS COMPONENT INSERTER EXTRACTOR 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 K870844.
When did SCHULTZ PROSTHESIS COMPONENT INSERTER EXTRACTOR receive FDA 510(k) clearance?
SCHULTZ PROSTHESIS COMPONENT INSERTER EXTRACTOR received FDA 510(k) clearance on 1987-03-13, under 510(k) number K870844.
Who is the listed applicant for SCHULTZ PROSTHESIS COMPONENT INSERTER EXTRACTOR?
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 PROSTHESIS COMPONENT INSERTER EXTRACTOR?
The FDA product code for SCHULTZ PROSTHESIS COMPONENT INSERTER EXTRACTOR is HWB.
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.
Related Devices (Code: HWB)
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.
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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