MAUDE data represents reports of adverse events involving medical devices. This maude entry was filed from a foreign,health professional report with the FDA on 2018-02-28 for ARGUS II RETINAL PROSTHESIS 011015-001 011015 manufactured by Second Sight Medical Products, Inc..
[101234178]
All pertinent information available to second sight medical products, inc. Has been submitted. The company is submitting this mdr to ensure full compliance with 21 cfr part 803.
Patient Sequence No: 1, Text Type: N, H10
[101234179]
This patient was implanted with the argus ii device on (b)(6) 2018. On (b)(6) 2018, this patient was diagnosed with conjunctival dehiscence in the implanted eye. Intraocular pressure (iop) in the implanted eye was 21 mmhg. The surgeon closed the conjunctival dehiscence with additional sutures. On (b)(6) 2018, recurrent conjunctival dehiscence was observed in the implanted eye and iop in the implanted eye was 30 mmhg. Patient had been on prescribed glaucoma eye drops since (b)(6) 2018. On (b)(6) 2018, conjunctival autograft harvested from the fellow eye was sutured over the conjunctival dehiscence in the implanted eye. On (b)(6) 2018, the surgeon reported that the patient's conjunctiva was fully closed and iop in the implanted eye was 16 mmhg. Patient is continuing the prescribed eye drops. There was no defect or malfunction of the device associated with this event.
Patient Sequence No: 1, Text Type: D, B5
| Report Number | 3004081696-2018-00003 |
| MDR Report Key | 7304550 |
| Report Source | FOREIGN,HEALTH PROFESSIONAL |
| Date Received | 2018-02-28 |
| Date of Report | 2018-01-29 |
| Date of Event | 2018-01-29 |
| Date Mfgr Received | 2018-01-29 |
| Device Manufacturer Date | 2017-06-21 |
| Date Added to Maude | 2018-02-28 |
| Event Key | 0 |
| Report Source Code | Manufacturer report |
| Manufacturer Link | Y |
| Number of Patients in Event | 0 |
| Adverse Event Flag | 3 |
| Product Problem Flag | 3 |
| Reprocessed and Reused Flag | 3 |
| Health Professional | 3 |
| Initial Report to FDA | 3 |
| Report to FDA | 3 |
| Event Location | 3 |
| Manufacturer Contact | MR. MARK LOAR |
| Manufacturer Street | 12744 SAN FERNANDO RD. SUITE 400 |
| Manufacturer City | SYLMAR CA 91342 |
| Manufacturer Country | US |
| Manufacturer Postal | 91342 |
| Manufacturer Phone | 8188335049 |
| Manufacturer G1 | SECOND SIGHT MEDICAL PRODUCTS, INC. |
| Manufacturer Street | 12744 SAN FERNANDO RD. SUITE 400 |
| Manufacturer City | SYLMAR CA 91342 |
| Manufacturer Country | US |
| Manufacturer Postal Code | 91342 |
| Single Use | 3 |
| Previous Use Code | 3 |
| Event Type | 3 |
| Type of Report | 3 |
| Brand Name | ARGUS II RETINAL PROSTHESIS |
| Generic Name | RETINAL PROSTHESIS |
| Product Code | NBF |
| Date Received | 2018-02-28 |
| Model Number | 011015-001 |
| Catalog Number | 011015 |
| Lot Number | N/A |
| Device Expiration Date | 2019-06-21 |
| Operator | PHYSICIAN |
| Device Availability | N |
| Device Eval'ed by Mfgr | R |
| Device Sequence No | 1 |
| Device Event Key | 0 |
| Manufacturer | SECOND SIGHT MEDICAL PRODUCTS, INC. |
| Manufacturer Address | 12744 SAN FERNANDO RD. SUITE 400 SYLMAR CA 91342 US 91342 |
| Patient Number | Treatment | Outcome | Date |
|---|---|---|---|
| 1 | 0 | 1. Required No Informationntervention | 2018-02-28 |