ORTHOCOR ACTIVE DEVICE ORTHOCOR GENERAL USE ACTIVE DEVICE— 510(k) K121702
Substantially EquivalentOrthocor Medical
FDA 510(k) clearance K121702 for ORTHOCOR ACTIVE DEVICE ORTHOCOR GENERAL USE ACTIVE DEVICE, Substantially Equivalent on 2013-05-06. Applicant: Orthocor Medical. Device class: 2.
Clearance details
- Applicant
- Orthocor Medical
- Product code
- Code ILX
- Device class
- Class 2
- Regulation
- 21 CFR 890.5290
- Advisory panel
- Physical Medicine
- Date received
- Decision date
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Location
- Ashland, MA, US
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