Spine CAMP™
K-Number: K221632 · 2022-10-18
Device Summary
Frequently Asked Questions
What is the Spine CAMP™?
Spine CAMP™ is a medical device that received FDA 510(k) clearance on 2022-10-18. The listed applicant is Medical Metrics, Inc.. The 510(k) number is K221632.
When did Spine CAMP™ receive FDA 510(k) clearance?
Spine CAMP™ received FDA 510(k) clearance on 2022-10-18, under 510(k) number K221632.
Who is the listed applicant for Spine CAMP™?
The FDA 510(k) record lists Medical Metrics, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for Spine CAMP™?
The FDA product code for Spine CAMP™ is QIH.
Other records listing Medical Metrics, 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: QIH)
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.