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FDA 510(k), K852137, FENLIN TOTAL SHOULDER
FDA 510(k), K852137, FENLIN TOTAL SHOULDER
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510(K) Number: K852137
Device Name: FENLIN TOTAL SHOULDER
Manufacturer: MAX SHERMAN
Device Classification Name:
Regulation Number:
Classification Product Code: KXA
Date Received: 05/16/1985
Decision Date: 02/12/1986
Decision: Substantially Equivalent (SESE)
Regulation Medical Specialty: Orthopedic
Device Name: FENLIN TOTAL SHOULDER
Manufacturer: MAX SHERMAN
Device Classification Name:
Regulation Number:
Classification Product Code: KXA
Date Received: 05/16/1985
Decision Date: 02/12/1986
Decision: Substantially Equivalent (SESE)
Regulation Medical Specialty: Orthopedic
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- Delivery: Approximately 1 to 2 weeks when the FOIA office is operating at regular capacity
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